11-3392190-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392190
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392190
    reference: chr 11
allele count: 5
allele frequency: 4.140375283615707e-5
allele num: 120762
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.412+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.238+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.*1A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.226+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.320+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.238+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.238+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.238+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.226+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434361
  ensembl transcript: ENST00000529228
  gene symbol: ZNF195
  hgvsc: ENST00000529228.1:c.97+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.226+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.238+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.238+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.226+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.391+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.238+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.226+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.173+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.238+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.238+15A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.226+15A>G
  variant of: http://identifiers.org/hgnc/12986
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-3392193-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392193
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392193
    reference: chr 11
allele count: 3
allele frequency: 2.483978339708878e-5
allele num: 120774
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.226+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434361
  ensembl transcript: ENST00000529228
  gene symbol: ZNF195
  hgvsc: ENST00000529228.1:c.97+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.238+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.238+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.238+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.226+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.226+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.226+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.226+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.226+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.271+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.173+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.226+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.320+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.226+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.238+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: stop_lost
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.238T>G
  hgvsp: ENSP00000435741.1:p.Ter80GlyextTer39
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.238+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.391+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.238+12T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.238+12T>G
  variant of: http://identifiers.org/hgnc/12986
canonical: false
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ter80GlyextTer39
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

11-3392196-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392196
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392196
    reference: chr 11
allele count: 1
allele frequency: 8.279516476237788e-6
allele num: 120780
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.226+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.238+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.226+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.238+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.226+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434361
  ensembl transcript: ENST00000529228
  gene symbol: ZNF195
  hgvsc: ENST00000529228.1:c.97+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.226+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.238+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.173+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.235G>C
  hgvsp: ENSP00000435741.1:p.Glu79Gln
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.391+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.226+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.238+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.271+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.226+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.238+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.238+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.238+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.226+9G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.238+9G>C
  variant of: http://identifiers.org/hgnc/12986
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu79Gln
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

11-3392202-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392202
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392202
    reference: chr 11
allele count: 2
allele frequency: 1.655464688938185e-5
allele num: 120812
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434361
  ensembl transcript: ENST00000529228
  gene symbol: ZNF195
  hgvsc: ENST00000529228.1:c.97+3G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.238+3G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.238+3G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.226+3G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.412+3G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.226+3G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.238+3G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.238+3G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.238+3G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.226+3G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.229G>A
  hgvsp: ENSP00000435741.1:p.Gly77Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.238+3G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.320+3G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.226+3G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.226+3G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.226+3G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.226+3G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.271+3G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.238+3G>A
  variant of: http://identifiers.org/hgnc/12986
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly77Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

11-3392206-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392206
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392206
    reference: chr 11
allele count: 14
allele frequency: 1.158786915640313e-4
allele num: 120816
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.237A>G
  hgvsp: ENST00000429541.2:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.225A>G
  hgvsp: ENST00000530643.1:c.225A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.237A>G
  hgvsp: ENST00000534569.1:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.225A>G
  hgvsp: ENST00000533036.1:c.225A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.225A>G
  hgvsp: ENST00000354599.6:c.225A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.237A>G
  hgvsp: ENST00000529678.1:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.225A>G
  hgvsp: ENST00000526501.1:c.225A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.237A>G
  hgvsp: ENST00000526601.1:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434361
  ensembl transcript: ENST00000529228
  gene symbol: ZNF195
  hgvsc: ENST00000529228.1:c.96A>G
  hgvsp: ENST00000529228.1:c.96A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.225A>G
  hgvsp: ENST00000525502.1:c.225A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.237A>G
  hgvsp: ENST00000343338.7:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.225A>G
  hgvsp: ENST00000528796.1:c.225A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.319A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.237A>G
  hgvsp: ENST00000438262.2:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.237A>G
  hgvsp: ENST00000532539.1:c.237A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.390A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.270A>G
  hgvsp: ENST00000427810.2:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.225A>G
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-3392211-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392211
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392211
    reference: chr 11
allele count: 2
allele frequency: 1.655327672112695e-5
allele num: 120822
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.220C>T
  hgvsp: ENSP00000432720.1:p.His74Tyr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.220C>T
  hgvsp: ENSP00000005082.9:p.His74Tyr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.220C>T
  hgvsp: ENSP00000382511.4:p.His74Tyr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.220C>T
  hgvsp: ENSP00000346613.6:p.His74Tyr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.265C>T
  hgvsp: ENSP00000390663.2:p.His89Tyr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.232C>T
  hgvsp: ENSP00000434715.1:p.His78Tyr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.232C>T
  hgvsp: ENSP00000435153.1:p.His78Tyr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.232C>T
  hgvsp: ENSP00000431937.1:p.His78Tyr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.232C>T
  hgvsp: ENSP00000414353.2:p.His78Tyr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.232C>T
  hgvsp: ENSP00000436384.1:p.His78Tyr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.314C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.220C>T
  hgvsp: ENSP00000432552.1:p.His74Tyr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.232C>T
  hgvsp: ENSP00000435828.1:p.His78Tyr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.220C>T
  hgvsp: ENSP00000435741.1:p.His74Tyr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.406C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.232C>T
  hgvsp: ENSP00000437265.1:p.His78Tyr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.220C>T
  hgvsp: ENSP00000433911.1:p.His74Tyr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.220C>T
  hgvsp: ENSP00000435093.1:p.His74Tyr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434361
  ensembl transcript: ENST00000529228
  gene symbol: ZNF195
  hgvsc: ENST00000529228.1:c.91C>T
  hgvsp: ENSP00000434361.1:p.His31Tyr
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.His74Tyr
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

11-3392211-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392211
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392211
    reference: chr 11
allele count: 12
allele frequency: 9.931966032676168e-5
allele num: 120822
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434361
  ensembl transcript: ENST00000529228
  gene symbol: ZNF195
  hgvsc: ENST00000529228.1:c.91C>A
  hgvsp: ENSP00000434361.1:p.His31Asn
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.232C>A
  hgvsp: ENSP00000414353.2:p.His78Asn
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.232C>A
  hgvsp: ENSP00000436384.1:p.His78Asn
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.232C>A
  hgvsp: ENSP00000431937.1:p.His78Asn
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.385C>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.232C>A
  hgvsp: ENSP00000435828.1:p.His78Asn
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.232C>A
  hgvsp: ENSP00000387998.2:p.His78Asn
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.232C>A
  hgvsp: ENSP00000437265.1:p.His78Asn
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.220C>A
  hgvsp: ENSP00000433911.1:p.His74Asn
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.580C>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.265C>A
  hgvsp: ENSP00000390663.2:p.His89Asn
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.220C>A
  hgvsp: ENSP00000382511.4:p.His74Asn
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.220C>A
  hgvsp: ENSP00000005082.9:p.His74Asn
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.232C>A
  hgvsp: ENSP00000434715.1:p.His78Asn
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.220C>A
  hgvsp: ENSP00000434006.1:p.His74Asn
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.220C>A
  hgvsp: ENSP00000435093.1:p.His74Asn
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.314C>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.232C>A
  hgvsp: ENSP00000435153.1:p.His78Asn
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.406C>A
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.His74Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

11-3392214-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392214
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392214
    reference: chr 11
allele count: 2
allele frequency: 1.655300271469245e-5
allele num: 120824
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.217G>A
  hgvsp: ENSP00000432552.1:p.Gly73Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.229G>A
  hgvsp: ENSP00000435828.1:p.Gly77Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.217G>A
  hgvsp: ENSP00000435741.1:p.Gly73Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.262G>A
  hgvsp: ENSP00000390663.2:p.Gly88Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.229G>A
  hgvsp: ENSP00000437265.1:p.Gly77Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.382G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.229G>A
  hgvsp: ENSP00000387998.2:p.Gly77Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.229G>A
  hgvsp: ENSP00000434715.1:p.Gly77Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.217G>A
  hgvsp: ENSP00000435093.1:p.Gly73Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.217G>A
  hgvsp: ENSP00000346613.6:p.Gly73Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.229G>A
  hgvsp: ENSP00000436384.1:p.Gly77Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.229G>A
  hgvsp: ENSP00000431937.1:p.Gly77Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.217G>A
  hgvsp: ENSP00000432720.1:p.Gly73Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.217G>A
  hgvsp: ENSP00000005082.9:p.Gly73Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.577G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.229G>A
  hgvsp: ENSP00000414353.2:p.Gly77Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.311G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.164G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434361
  ensembl transcript: ENST00000529228
  gene symbol: ZNF195
  hgvsc: ENST00000529228.1:c.88G>A
  hgvsp: ENSP00000434361.1:p.Gly30Arg
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly73Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-3392215-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392215
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392215
    reference: chr 11
allele count: 12
allele frequency: 9.931637230397431e-5
allele num: 120826
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.216C>T
  hgvsp: ENST00000005082.9:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.216C>T
  hgvsp: ENST00000525502.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.261C>T
  hgvsp: ENST00000427810.2:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.216C>T
  hgvsp: ENST00000533036.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.216C>T
  hgvsp: ENST00000526501.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.228C>T
  hgvsp: ENST00000532539.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.228C>T
  hgvsp: ENST00000429541.2:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.216C>T
  hgvsp: ENST00000354599.6:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.228C>T
  hgvsp: ENST00000529678.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.228C>T
  hgvsp: ENST00000528410.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.228C>T
  hgvsp: ENST00000534569.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.381C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.228C>T
  hgvsp: ENST00000526601.1:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.216C>T
  hgvsp: ENST00000399602.4:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.310C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.216C>T
  hgvsp: ENST00000530643.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.576C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.228C>T
  hgvsp: ENST00000343338.7:c.228C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.216C>T
  hgvsp: ENST00000525313.2:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp72Asp
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ

11-3392224-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392224
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392224
    reference: chr 11
allele count: 2
allele frequency: 1.655190677966102e-5
allele num: 120832
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.219G>A
  hgvsp: ENST00000526601.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.219G>A
  hgvsp: ENST00000343338.7:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.207G>A
  hgvsp: ENST00000005082.9:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.219G>A
  hgvsp: ENST00000532539.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.219G>A
  hgvsp: ENST00000529678.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.219G>A
  hgvsp: ENST00000438262.2:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.207G>A
  hgvsp: ENST00000525313.2:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.219G>A
  hgvsp: ENST00000528410.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.154G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.207G>A
  hgvsp: ENST00000533036.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.219G>A
  hgvsp: ENST00000429541.2:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.219G>A
  hgvsp: ENST00000528218.1:c.219G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434361
  ensembl transcript: ENST00000529228
  gene symbol: ZNF195
  hgvsc: ENST00000529228.1:c.78G>A
  hgvsp: ENST00000529228.1:c.78G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.207G>A
  hgvsp: ENST00000530643.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.301G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.207G>A
  hgvsp: ENST00000399602.4:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.207G>A
  hgvsp: ENST00000528796.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.252G>A
  hgvsp: ENST00000427810.2:c.252G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.207G>A
  hgvsp: ENST00000525502.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Glu69Glu
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

11-3392227-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392227
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392227
    reference: chr 11
allele count: 1
allele frequency: 8.275816409288777e-6
allele num: 120834
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.216G>A
  hgvsp: ENST00000429541.2:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.204G>A
  hgvsp: ENST00000399602.4:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.216G>A
  hgvsp: ENST00000534569.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.204G>A
  hgvsp: ENST00000005082.9:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.204G>A
  hgvsp: ENST00000525502.1:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.298G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.216G>A
  hgvsp: ENST00000528410.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.204G>A
  hgvsp: ENST00000530643.1:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.216G>A
  hgvsp: ENST00000528218.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.216G>A
  hgvsp: ENST00000343338.7:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.216G>A
  hgvsp: ENST00000532539.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.216G>A
  hgvsp: ENST00000438262.2:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.204G>A
  hgvsp: ENST00000354599.6:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.216G>A
  hgvsp: ENST00000526601.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.204G>A
  hgvsp: ENST00000526501.1:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.216G>A
  hgvsp: ENST00000529678.1:c.216G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.151G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.204G>A
  hgvsp: ENST00000528796.1:c.204G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.390G>A
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gln68Gln
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

11-3392234-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392234
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392234
    reference: chr 11
allele count: 2
allele frequency: 1.655108492361674e-5
allele num: 120838
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.197A>G
  hgvsp: ENSP00000432720.1:p.Lys66Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.209A>G
  hgvsp: ENSP00000435828.1:p.Lys70Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.197A>G
  hgvsp: ENSP00000434006.1:p.Lys66Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.209A>G
  hgvsp: ENSP00000387998.2:p.Lys70Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.291A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.209A>G
  hgvsp: ENSP00000431937.1:p.Lys70Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.362A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.209A>G
  hgvsp: ENSP00000434715.1:p.Lys70Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.209A>G
  hgvsp: ENSP00000344483.7:p.Lys70Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.197A>G
  hgvsp: ENSP00000346613.6:p.Lys66Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.209A>G
  hgvsp: ENSP00000437265.1:p.Lys70Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.209A>G
  hgvsp: ENSP00000414353.2:p.Lys70Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.209A>G
  hgvsp: ENSP00000435153.1:p.Lys70Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.197A>G
  hgvsp: ENSP00000435093.1:p.Lys66Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.242A>G
  hgvsp: ENSP00000390663.2:p.Lys81Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.197A>G
  hgvsp: ENSP00000005082.9:p.Lys66Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434361
  ensembl transcript: ENST00000529228
  gene symbol: ZNF195
  hgvsc: ENST00000529228.1:c.68A>G
  hgvsp: ENSP00000434361.1:p.Lys23Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.197A>G
  hgvsp: ENSP00000435741.1:p.Lys66Arg
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.197A>G
  hgvsp: ENSP00000433911.1:p.Lys66Arg
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys66Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

11-3392255-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392255
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392255
    reference: chr 11
allele count: 7
allele frequency: 5.793167372881356e-5
allele num: 120832
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.362G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.176G>A
  hgvsp: ENSP00000435093.1:p.Arg59Gln
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.188G>A
  hgvsp: ENSP00000431937.1:p.Arg63Gln
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.188G>A
  hgvsp: ENSP00000436384.1:p.Arg63Gln
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.341G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.188G>A
  hgvsp: ENSP00000414353.2:p.Arg63Gln
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.176G>A
  hgvsp: ENSP00000435741.1:p.Arg59Gln
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.123G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.176G>A
  hgvsp: ENSP00000433911.1:p.Arg59Gln
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.221G>A
  hgvsp: ENSP00000390663.2:p.Arg74Gln
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.176G>A
  hgvsp: ENSP00000346613.6:p.Arg59Gln
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434361
  ensembl transcript: ENST00000529228
  gene symbol: ZNF195
  hgvsc: ENST00000529228.1:c.47G>A
  hgvsp: ENSP00000434361.1:p.Arg16Gln
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.188G>A
  hgvsp: ENSP00000435828.1:p.Arg63Gln
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.188G>A
  hgvsp: ENSP00000435153.1:p.Arg63Gln
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.176G>A
  hgvsp: ENSP00000432720.1:p.Arg59Gln
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.176G>A
  hgvsp: ENSP00000005082.9:p.Arg59Gln
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.188G>A
  hgvsp: ENSP00000387998.2:p.Arg63Gln
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.270G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.188G>A
  hgvsp: ENSP00000437265.1:p.Arg63Gln
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg59Gln
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

11-3392256-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392256
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392256
    reference: chr 11
allele count: 2
allele frequency: 1.655272871732905e-5
allele num: 120826
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.175C>A
  hgvsp: ENST00000533036.1:c.175C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434361
  ensembl transcript: ENST00000529228
  gene symbol: ZNF195
  hgvsc: ENST00000529228.1:c.46C>A
  hgvsp: ENST00000529228.1:c.46C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.187C>A
  hgvsp: ENST00000528218.1:c.187C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.187C>A
  hgvsp: ENST00000526601.1:c.187C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.175C>A
  hgvsp: ENST00000354599.6:c.175C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.175C>A
  hgvsp: ENST00000526501.1:c.175C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.269C>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.187C>A
  hgvsp: ENST00000528410.1:c.187C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.535C>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.175C>A
  hgvsp: ENST00000525502.1:c.175C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.187C>A
  hgvsp: ENST00000343338.7:c.187C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.220C>A
  hgvsp: ENST00000427810.2:c.220C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.187C>A
  hgvsp: ENST00000532539.1:c.187C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.187C>A
  hgvsp: ENST00000438262.2:c.187C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.175C>A
  hgvsp: ENST00000005082.9:c.175C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.187C>A
  hgvsp: ENST00000529678.1:c.187C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.340C>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.361C>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.122C>A
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Arg59Arg
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ

11-3392266-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392266
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392266
    reference: chr 11
allele count: 2
allele frequency: 1.655355073663301e-5
allele num: 120820
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.177C>T
  hgvsp: ENST00000532539.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.165C>T
  hgvsp: ENST00000399602.4:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.177C>T
  hgvsp: ENST00000528410.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.177C>T
  hgvsp: ENST00000429541.2:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.330C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.177C>T
  hgvsp: ENST00000343338.7:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.177C>T
  hgvsp: ENST00000534569.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.165C>T
  hgvsp: ENST00000530643.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.165C>T
  hgvsp: ENST00000525313.2:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.177C>T
  hgvsp: ENST00000438262.2:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.177C>T
  hgvsp: ENST00000526601.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.210C>T
  hgvsp: ENST00000427810.2:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.165C>T
  hgvsp: ENST00000005082.9:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.177C>T
  hgvsp: ENST00000528218.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.165C>T
  hgvsp: ENST00000533036.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.165C>T
  hgvsp: ENST00000525502.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.112C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434361
  ensembl transcript: ENST00000529228
  gene symbol: ZNF195
  hgvsc: ENST00000529228.1:c.36C>T
  hgvsp: ENST00000529228.1:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.165C>T
  hgvsp: ENST00000526501.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Cys55Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
reference allele: G
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

11-3392273-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392273
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392273
    reference: chr 11
allele count: 1
allele frequency: 8.27787159365584e-6
allele num: 120804
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.170T>C
  hgvsp: ENSP00000435153.1:p.Ile57Thr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.105T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.170T>C
  hgvsp: ENSP00000344483.7:p.Ile57Thr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.344T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.158T>C
  hgvsp: ENSP00000432552.1:p.Ile53Thr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.170T>C
  hgvsp: ENSP00000436384.1:p.Ile57Thr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.170T>C
  hgvsp: ENSP00000387998.2:p.Ile57Thr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.170T>C
  hgvsp: ENSP00000437265.1:p.Ile57Thr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.158T>C
  hgvsp: ENSP00000435741.1:p.Ile53Thr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.158T>C
  hgvsp: ENSP00000005082.9:p.Ile53Thr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.170T>C
  hgvsp: ENSP00000435828.1:p.Ile57Thr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434361
  ensembl transcript: ENST00000529228
  gene symbol: ZNF195
  hgvsc: ENST00000529228.1:c.29T>C
  hgvsp: ENSP00000434361.1:p.Ile10Thr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.170T>C
  hgvsp: ENSP00000431937.1:p.Ile57Thr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.158T>C
  hgvsp: ENSP00000434006.1:p.Ile53Thr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.518T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.170T>C
  hgvsp: ENSP00000414353.2:p.Ile57Thr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.203T>C
  hgvsp: ENSP00000390663.2:p.Ile68Thr
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.252T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.323T>C
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile53Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP

11-3392283-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392283
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392283
    reference: chr 11
allele count: 1
allele frequency: 8.280750567231414e-6
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.148C>T
  hgvsp: ENSP00000432720.1:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.160C>T
  hgvsp: ENSP00000435153.1:p.Pro54Ser
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.148C>T
  hgvsp: ENSP00000432552.1:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.160C>T
  hgvsp: ENSP00000344483.7:p.Pro54Ser
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.148C>T
  hgvsp: ENSP00000005082.9:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.193C>T
  hgvsp: ENSP00000390663.2:p.Pro65Ser
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.148C>T
  hgvsp: ENSP00000433911.1:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.148C>T
  hgvsp: ENSP00000346613.6:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.160C>T
  hgvsp: ENSP00000387998.2:p.Pro54Ser
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.313C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.160C>T
  hgvsp: ENSP00000435828.1:p.Pro54Ser
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.160C>T
  hgvsp: ENSP00000431937.1:p.Pro54Ser
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.148C>T
  hgvsp: ENSP00000435093.1:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.334C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.160C>T
  hgvsp: ENSP00000436384.1:p.Pro54Ser
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.148C>T
  hgvsp: ENSP00000382511.4:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.160C>T
  hgvsp: ENSP00000434715.1:p.Pro54Ser
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.242C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.148C>T
  hgvsp: ENSP00000435741.1:p.Pro50Ser
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Pro50Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-3392288-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392288
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392288
    reference: chr 11
allele count: 1
allele frequency: 8.283906027370025e-6
allele num: 120716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.143G>T
  hgvsp: ENSP00000346613.6:p.Cys48Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.143G>T
  hgvsp: ENSP00000433911.1:p.Cys48Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.143G>T
  hgvsp: ENSP00000432720.1:p.Cys48Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.188G>T
  hgvsp: ENSP00000390663.2:p.Cys63Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.143G>T
  hgvsp: ENSP00000382511.4:p.Cys48Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.143G>T
  hgvsp: ENSP00000434006.1:p.Cys48Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.155G>T
  hgvsp: ENSP00000431937.1:p.Cys52Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.155G>T
  hgvsp: ENSP00000435828.1:p.Cys52Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.143G>T
  hgvsp: ENSP00000005082.9:p.Cys48Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.155G>T
  hgvsp: ENSP00000436384.1:p.Cys52Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.329G>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.155G>T
  hgvsp: ENSP00000387998.2:p.Cys52Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.308G>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.143G>T
  hgvsp: ENSP00000432552.1:p.Cys48Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.155G>T
  hgvsp: ENSP00000414353.2:p.Cys52Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.143G>T
  hgvsp: ENSP00000435093.1:p.Cys48Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434361
  ensembl transcript: ENST00000529228
  gene symbol: ZNF195
  hgvsc: ENST00000529228.1:c.14G>T
  hgvsp: ENSP00000434361.1:p.Cys5Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.237G>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.155G>T
  hgvsp: ENSP00000344483.7:p.Cys52Phe
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Cys48Phe
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

11-3392292-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392292
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392292
    reference: chr 11
allele count: 1
allele frequency: 8.286514526259965e-6
allele num: 120678
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.151G>C
  hgvsp: ENSP00000435153.1:p.Val51Leu
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.151G>C
  hgvsp: ENSP00000414353.2:p.Val51Leu
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.86G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.139G>C
  hgvsp: ENSP00000005082.9:p.Val47Leu
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.151G>C
  hgvsp: ENSP00000387998.2:p.Val51Leu
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.139G>C
  hgvsp: ENSP00000432720.1:p.Val47Leu
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.139G>C
  hgvsp: ENSP00000435093.1:p.Val47Leu
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.304G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434361
  ensembl transcript: ENST00000529228
  gene symbol: ZNF195
  hgvsc: ENST00000529228.1:c.10G>C
  hgvsp: ENSP00000434361.1:p.Val4Leu
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.139G>C
  hgvsp: ENSP00000346613.6:p.Val47Leu
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.325G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.151G>C
  hgvsp: ENSP00000431937.1:p.Val51Leu
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.139G>C
  hgvsp: ENSP00000435741.1:p.Val47Leu
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.499G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.151G>C
  hgvsp: ENSP00000436384.1:p.Val51Leu
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.151G>C
  hgvsp: ENSP00000437265.1:p.Val51Leu
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.151G>C
  hgvsp: ENSP00000435828.1:p.Val51Leu
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.151G>C
  hgvsp: ENSP00000434715.1:p.Val51Leu
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.139G>C
  hgvsp: ENSP00000433911.1:p.Val47Leu
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val47Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD

11-3392304-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392304
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392304
    reference: chr 11
allele count: 1
allele frequency: 8.303027283747654e-6
allele num: 120438
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.143-4A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.296-4A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.131-4A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.131-4A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.143-4A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.143-4A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.143-4A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.131-4A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.74A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.225-4A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.131-4A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.131-4A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.131-4A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.491-4A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.131-4A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.131-4A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.143-4A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.143-4A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.143-4A>T
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.131-4A>T
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

11-3392306-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392306
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392306
    reference: chr 11
allele count: 1
allele frequency: 8.304406317992327e-6
allele num: 120418
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.131-6A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.143-6A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.491-6A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.131-6A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.131-6A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.131-6A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.131-6A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.143-6A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.143-6A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.143-6A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.131-6A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.143-6A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.296-6A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.131-6A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.131-6A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.225-6A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.72A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.176-6A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.143-6A>C
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.131-6A>C
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD

11-3392307-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392307
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392307
    reference: chr 11
allele count: 2
allele frequency: 1.660991611992359e-5
allele num: 120410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.143-7A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.225-7A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.131-7A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.491-7A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.131-7A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.317-7A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.131-7A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.143-7A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.143-7A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.176-7A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.143-7A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.143-7A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.131-7A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.131-7A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.71A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.143-7A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.131-7A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.143-7A>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.143-7A>C
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.131-7A>C
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

11-3392308-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392308
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392308
    reference: chr 11
allele count: 1
allele frequency: 8.307855908547122e-6
allele num: 120368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.131-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.491-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.143-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.143-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.131-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.131-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.296-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.143-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.131-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.143-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.131-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.131-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.143-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.143-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.143-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.225-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.143-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.176-8T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.70T>C
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.131-8T>C
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

11-3392313-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392313
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392313
    reference: chr 11
allele count: 12
allele frequency: 9.976720984369804e-5
allele num: 120280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.143-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.131-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.131-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.131-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.131-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.131-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.131-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.143-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.143-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.296-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.143-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.143-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.131-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.143-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.317-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.131-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.143-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.176-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.65T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.143-13T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.131-13T>C
  variant of: http://identifiers.org/hgnc/12986
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

11-3392318-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392318
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392318
    reference: chr 11
allele count: 1
allele frequency: 8.320713584396998e-6
allele num: 120182
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.296-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.143-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.143-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.131-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.131-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.143-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.131-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.143-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.131-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.131-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.176-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.143-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.143-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.60T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.131-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.491-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.225-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.143-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.143-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.131-18T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.131-18T>C
  variant of: http://identifiers.org/hgnc/12986
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

11-3392331-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392331
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392331
    reference: chr 11
allele count: 2
allele frequency: 1.668975415992122e-5
allele num: 119834
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.143-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.131-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.47A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.491-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.131-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.131-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.131-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.131-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.143-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.143-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.317-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.176-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.143-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.131-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.143-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.131-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.143-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.296-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.225-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.131-31A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.131-31A>G
  variant of: http://identifiers.org/hgnc/12986
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: T
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-3392347-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392347
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392347
    reference: chr 11
allele count: 1
allele frequency: 8.400537634408602e-6
allele num: 119040
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.143-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.143-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.143-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.131-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.131-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.131-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.131-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.131-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.131-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.31T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.131-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.131-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.143-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.296-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.491-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.143-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.225-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.143-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.131-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.176-47T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.317-47T>C
  variant of: http://identifiers.org/hgnc/12986
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-3392351-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392351
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392351
    reference: chr 11
allele count: 88335
allele frequency: 7.463752196836555e-1
allele num: 118352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.131-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.143-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529789
  gene symbol: ZNF195
  hgvsc: ENST00000529789.1:n.27A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.131-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.143-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.131-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.131-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.143-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.491-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.143-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.131-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.131-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.131-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.131-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.143-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.143-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.143-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.143-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.296-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.225-51A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.143-51A>G
  variant of: http://identifiers.org/hgnc/12986
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 33193
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

11-3392759-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392759
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392759
    reference: chr 11
allele count: 10
allele frequency: 8.283082632032337e-5
allele num: 120728
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.142+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.142+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.130+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.142+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.130+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.130+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.142+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.142+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.130+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.295+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.142+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.130+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.490+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.142+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.224+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.130+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.316+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.130+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.130+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.130+48C>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.175+48C>G
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-3392762-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392762
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392762
    reference: chr 11
allele count: 5
allele frequency: 4.140992513085536e-5
allele num: 120744
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.130+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.142+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.130+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.130+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.175+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.130+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.130+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.142+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.142+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.316+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.224+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.142+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.130+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.142+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.490+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.142+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.130+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.142+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.130+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.130+45T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.142+45T>A
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS

11-3392772-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392772
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392772
    reference: chr 11
allele count: 1
allele frequency: 8.282945415389712e-6
allele num: 120730
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.142+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.490+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.142+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.142+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.142+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.130+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.130+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.130+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.142+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.130+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.130+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.224+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.142+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.295+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.130+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.142+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.130+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.142+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.130+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.130+35C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.175+35C>T
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

11-3392786-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392786
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392786
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 120764
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.130+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.224+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.142+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.142+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.316+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.142+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.142+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.142+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.175+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.490+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.130+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.130+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.142+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.130+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.130+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.130+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.130+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.130+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.142+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.142+21T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.130+21T>C
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

11-3392787-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392787
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392787
    reference: chr 11
allele count: 2
allele frequency: 1.656342134031205e-5
allele num: 120748
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.295+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.130+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.130+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.142+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.142+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.224+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.130+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.142+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.130+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.130+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.142+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.490+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.130+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.142+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.175+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.142+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.130+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.130+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.142+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.142+20G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.316+20G>A
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
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: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

11-3392788-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392788
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392788
    reference: chr 11
allele count: 2
allele frequency: 1.656122685568547e-5
allele num: 120764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.130+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.142+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.130+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.130+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.130+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.316+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.224+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.142+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.130+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.490+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.142+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.142+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.142+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.130+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.130+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.142+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.142+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.130+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.130+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.175+19C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.142+19C>T
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

11-3392791-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392791
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392791
    reference: chr 11
allele count: 1
allele frequency: 8.278693953241936e-6
allele num: 120792
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.130+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.490+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.142+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.130+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.130+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.142+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.130+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.130+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.130+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.175+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.130+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.295+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.142+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.224+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.142+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.142+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.130+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.142+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.142+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.130+16A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.142+16A>T
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

11-3392791-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392791
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392791
    reference: chr 11
allele count: 2
allele frequency: 1.655738790648387e-5
allele num: 120792
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.130+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.130+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.142+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.142+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.224+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.130+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.316+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.490+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.142+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.130+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.130+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.142+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.142+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.142+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.142+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.130+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.130+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.142+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.175+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.142+16A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.130+16A>G
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

11-3392800-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392800
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392800
    reference: chr 11
allele count: 3
allele frequency: 2.482909307599358e-5
allele num: 120826
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.142+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.130+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.142+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.224+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.142+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.142+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.130+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.130+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.130+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.142+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.130+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.142+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.130+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.175+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.295+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.490+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.130+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.130+7A>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.316+7A>T
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.130+7A>T
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

11-3392810-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392810
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392810
    reference: chr 11
allele count: 6
allele frequency: 4.964668111936717e-5
allele num: 120854
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.127G>A
  hgvsp: ENSP00000434006.1:p.Val43Ile
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.139G>A
  hgvsp: ENSP00000344483.7:p.Val47Ile
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.139G>A
  hgvsp: ENSP00000435153.1:p.Val47Ile
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.127G>A
  hgvsp: ENSP00000432552.1:p.Val43Ile
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.127G>A
  hgvsp: ENSP00000433911.1:p.Val43Ile
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.139G>A
  hgvsp: ENSP00000387998.2:p.Val47Ile
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.127G>A
  hgvsp: ENSP00000435093.1:p.Val43Ile
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.313G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.127G>A
  hgvsp: ENSP00000005082.9:p.Val43Ile
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.127G>A
  hgvsp: ENSP00000346613.6:p.Val43Ile
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.139G>A
  hgvsp: ENSP00000414353.2:p.Val47Ile
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.139G>A
  hgvsp: ENSP00000431937.1:p.Val47Ile
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.127G>A
  hgvsp: ENSP00000435741.1:p.Val43Ile
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.172G>A
  hgvsp: ENSP00000390663.2:p.Val58Ile
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.127G>A
  hgvsp: ENSP00000432720.1:p.Val43Ile
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.139G>A
  hgvsp: ENSP00000435828.1:p.Val47Ile
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.292G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.127G>A
  hgvsp: ENSP00000382511.4:p.Val43Ile
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.139G>A
  hgvsp: ENSP00000437265.1:p.Val47Ile
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val43Ile
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

11-3392811-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392811
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392811
    reference: chr 11
allele count: 2843
allele frequency: 2.35273672189212e-2
allele num: 120838
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.138C>T
  hgvsp: ENST00000438262.2:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.138C>T
  hgvsp: ENST00000528218.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.138C>T
  hgvsp: ENST00000534569.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.126C>T
  hgvsp: ENST00000525313.2:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.138C>T
  hgvsp: ENST00000528410.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.171C>T
  hgvsp: ENST00000427810.2:c.171C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.312C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.126C>T
  hgvsp: ENST00000526501.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.126C>T
  hgvsp: ENST00000528796.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.126C>T
  hgvsp: ENST00000525502.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.138C>T
  hgvsp: ENST00000529678.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.138C>T
  hgvsp: ENST00000343338.7:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.126C>T
  hgvsp: ENST00000005082.9:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.126C>T
  hgvsp: ENST00000530643.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.138C>T
  hgvsp: ENST00000526601.1:c.138C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.220C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.126C>T
  hgvsp: ENST00000399602.4:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.126C>T
  hgvsp: ENST00000533036.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.291C>T
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser42Ser
num of homozygotes: 54
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-3392815-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392815
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392815
    reference: chr 11
allele count: 18
allele frequency: 1.488907638096184e-4
allele num: 120894
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.122T>G
  hgvsp: ENSP00000434006.1:p.Phe41Cys
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.134T>G
  hgvsp: ENSP00000387998.2:p.Phe45Cys
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.167T>G
  hgvsp: ENSP00000390663.2:p.Phe56Cys
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.122T>G
  hgvsp: ENSP00000435093.1:p.Phe41Cys
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.122T>G
  hgvsp: ENSP00000005082.9:p.Phe41Cys
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.122T>G
  hgvsp: ENSP00000382511.4:p.Phe41Cys
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.134T>G
  hgvsp: ENSP00000414353.2:p.Phe45Cys
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.122T>G
  hgvsp: ENSP00000346613.6:p.Phe41Cys
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.134T>G
  hgvsp: ENSP00000434715.1:p.Phe45Cys
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.482T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.122T>G
  hgvsp: ENSP00000432720.1:p.Phe41Cys
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.134T>G
  hgvsp: ENSP00000435153.1:p.Phe45Cys
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.134T>G
  hgvsp: ENSP00000435828.1:p.Phe45Cys
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.308T>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.134T>G
  hgvsp: ENSP00000431937.1:p.Phe45Cys
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.122T>G
  hgvsp: ENSP00000432552.1:p.Phe41Cys
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.134T>G
  hgvsp: ENSP00000436384.1:p.Phe45Cys
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.134T>G
  hgvsp: ENSP00000344483.7:p.Phe45Cys
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.216T>G
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Phe41Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-3392820-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392820
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392820
    reference: chr 11
allele count: 2
allele frequency: 1.654232353476369e-5
allele num: 120902
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.117C>T
  hgvsp: ENST00000533036.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.129C>T
  hgvsp: ENST00000528218.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.117C>T
  hgvsp: ENST00000530643.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.129C>T
  hgvsp: ENST00000526601.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.129C>T
  hgvsp: ENST00000528410.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.129C>T
  hgvsp: ENST00000532539.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.211C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.162C>T
  hgvsp: ENST00000427810.2:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.477C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.117C>T
  hgvsp: ENST00000525313.2:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.117C>T
  hgvsp: ENST00000528796.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.117C>T
  hgvsp: ENST00000525502.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.117C>T
  hgvsp: ENST00000354599.6:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.129C>T
  hgvsp: ENST00000343338.7:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.117C>T
  hgvsp: ENST00000005082.9:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.282C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.129C>T
  hgvsp: ENST00000529678.1:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.129C>T
  hgvsp: ENST00000429541.2:c.129C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.117C>T
  hgvsp: ENST00000526501.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asn39Asn
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-3392853-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392853
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392853
    reference: chr 11
allele count: 1
allele frequency: 8.268836409340477e-6
allele num: 120936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.96G>T
  hgvsp: ENSP00000435153.1:p.Leu32Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.96G>T
  hgvsp: ENSP00000387998.2:p.Leu32Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.84G>T
  hgvsp: ENSP00000432720.1:p.Leu28Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.84G>T
  hgvsp: ENSP00000435093.1:p.Leu28Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.84G>T
  hgvsp: ENSP00000005082.9:p.Leu28Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.178G>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.96G>T
  hgvsp: ENSP00000434715.1:p.Leu32Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.129G>T
  hgvsp: ENSP00000390663.2:p.Leu43Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.84G>T
  hgvsp: ENSP00000432552.1:p.Leu28Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.96G>T
  hgvsp: ENSP00000344483.7:p.Leu32Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.96G>T
  hgvsp: ENSP00000437265.1:p.Leu32Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.84G>T
  hgvsp: ENSP00000346613.6:p.Leu28Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.84G>T
  hgvsp: ENSP00000433911.1:p.Leu28Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.96G>T
  hgvsp: ENSP00000414353.2:p.Leu32Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.96G>T
  hgvsp: ENSP00000436384.1:p.Leu32Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.96G>T
  hgvsp: ENSP00000431937.1:p.Leu32Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.84G>T
  hgvsp: ENSP00000435741.1:p.Leu28Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.96G>T
  hgvsp: ENSP00000435828.1:p.Leu32Phe
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.444G>T
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu28Phe
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

11-3392855-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392855
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392855
    reference: chr 11
allele count: 1
allele frequency: 8.269109913008963e-6
allele num: 120932
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.127T>C
  hgvsp: ENST00000427810.2:c.127T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.94T>C
  hgvsp: ENST00000526601.1:c.94T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.442T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.82T>C
  hgvsp: ENST00000526501.1:c.82T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.94T>C
  hgvsp: ENST00000528218.1:c.94T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.82T>C
  hgvsp: ENST00000354599.6:c.82T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.94T>C
  hgvsp: ENST00000534569.1:c.94T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.82T>C
  hgvsp: ENST00000530643.1:c.82T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.94T>C
  hgvsp: ENST00000438262.2:c.94T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.94T>C
  hgvsp: ENST00000528410.1:c.94T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.82T>C
  hgvsp: ENST00000528796.1:c.82T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.82T>C
  hgvsp: ENST00000005082.9:c.82T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.94T>C
  hgvsp: ENST00000532539.1:c.94T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.82T>C
  hgvsp: ENST00000399602.4:c.82T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.94T>C
  hgvsp: ENST00000429541.2:c.94T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.94T>C
  hgvsp: ENST00000529678.1:c.94T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.176T>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.82T>C
  hgvsp: ENST00000525502.1:c.82T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.94T>C
  hgvsp: ENST00000343338.7:c.94T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu28Leu
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

11-3392855-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392855
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392855
    reference: chr 11
allele count: 1
allele frequency: 8.269109913008963e-6
allele num: 120932
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.176T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.94T>A
  hgvsp: ENSP00000437265.1:p.Leu32Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.94T>A
  hgvsp: ENSP00000436384.1:p.Leu32Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.82T>A
  hgvsp: ENSP00000346613.6:p.Leu28Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.268T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.82T>A
  hgvsp: ENSP00000435741.1:p.Leu28Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.82T>A
  hgvsp: ENSP00000435093.1:p.Leu28Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.94T>A
  hgvsp: ENSP00000344483.7:p.Leu32Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.442T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.94T>A
  hgvsp: ENSP00000414353.2:p.Leu32Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.82T>A
  hgvsp: ENSP00000432552.1:p.Leu28Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.94T>A
  hgvsp: ENSP00000387998.2:p.Leu32Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.82T>A
  hgvsp: ENSP00000382511.4:p.Leu28Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.82T>A
  hgvsp: ENSP00000432720.1:p.Leu28Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.82T>A
  hgvsp: ENSP00000434006.1:p.Leu28Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.94T>A
  hgvsp: ENSP00000435153.1:p.Leu32Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.94T>A
  hgvsp: ENSP00000431937.1:p.Leu32Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.82T>A
  hgvsp: ENSP00000433911.1:p.Leu28Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.94T>A
  hgvsp: ENSP00000435828.1:p.Leu32Met
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu28Met
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

11-3392862-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392862
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392862
    reference: chr 11
allele count: 1
allele frequency: 8.270751315049459e-6
allele num: 120908
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.75G>A
  hgvsp: ENST00000530643.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.87G>A
  hgvsp: ENST00000343338.7:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.87G>A
  hgvsp: ENST00000534569.1:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.87G>A
  hgvsp: ENST00000532539.1:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.75G>A
  hgvsp: ENST00000525313.2:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.240G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.87G>A
  hgvsp: ENST00000526601.1:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.87G>A
  hgvsp: ENST00000528410.1:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.75G>A
  hgvsp: ENST00000533036.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.75G>A
  hgvsp: ENST00000399602.4:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.87G>A
  hgvsp: ENST00000529678.1:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.75G>A
  hgvsp: ENST00000005082.9:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.87G>A
  hgvsp: ENST00000528218.1:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.87G>A
  hgvsp: ENST00000429541.2:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.75G>A
  hgvsp: ENST00000525502.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.75G>A
  hgvsp: ENST00000526501.1:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.87G>A
  hgvsp: ENST00000438262.2:c.87G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.75G>A
  hgvsp: ENST00000354599.6:c.75G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.120G>A
  hgvsp: ENST00000427810.2:c.120G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gln25Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD

11-3392877-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392877
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392877
    reference: chr 11
allele count: 5
allele frequency: 4.137839716640736e-5
allele num: 120836
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.72C>T
  hgvsp: ENST00000532539.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.72C>T
  hgvsp: ENST00000528410.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.72C>T
  hgvsp: ENST00000528218.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.60C>T
  hgvsp: ENST00000005082.9:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.225C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.60C>T
  hgvsp: ENST00000525502.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.105C>T
  hgvsp: ENST00000427810.2:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.60C>T
  hgvsp: ENST00000528796.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.72C>T
  hgvsp: ENST00000438262.2:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.72C>T
  hgvsp: ENST00000526601.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.60C>T
  hgvsp: ENST00000526501.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.60C>T
  hgvsp: ENST00000530643.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.72C>T
  hgvsp: ENST00000429541.2:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.60C>T
  hgvsp: ENST00000399602.4:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.60C>T
  hgvsp: ENST00000525313.2:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.72C>T
  hgvsp: ENST00000343338.7:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.72C>T
  hgvsp: ENST00000534569.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.72C>T
  hgvsp: ENST00000529678.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.60C>T
  hgvsp: ENST00000354599.6:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Cys20Cys
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

11-3392892-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392892
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392892
    reference: chr 11
allele count: 8
allele frequency: 6.635039644361875e-5
allele num: 120572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.57G>A
  hgvsp: ENST00000532539.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.57G>A
  hgvsp: ENST00000528410.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.45G>A
  hgvsp: ENST00000399602.4:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.57G>A
  hgvsp: ENST00000429541.2:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.45G>A
  hgvsp: ENST00000530643.1:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.57G>A
  hgvsp: ENST00000528218.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.57G>A
  hgvsp: ENST00000534569.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.57G>A
  hgvsp: ENST00000526601.1:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.45G>A
  hgvsp: ENST00000526501.1:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.405G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.45G>A
  hgvsp: ENST00000525502.1:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.45G>A
  hgvsp: ENST00000354599.6:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.90G>A
  hgvsp: ENST00000427810.2:c.90G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.45G>A
  hgvsp: ENST00000525313.2:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.45G>A
  hgvsp: ENST00000528796.1:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.57G>A
  hgvsp: ENST00000438262.2:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.45G>A
  hgvsp: ENST00000005082.9:c.45G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.57G>A
  hgvsp: ENST00000343338.7:c.57G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.139G>A
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu15Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

11-3392910-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392910
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392910
    reference: chr 11
allele count: 1
allele frequency: 8.345852111500584e-6
allele num: 119820
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.27G>A
  hgvsp: ENST00000533036.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.27G>A
  hgvsp: ENST00000530643.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.39G>A
  hgvsp: ENST00000529678.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.39G>A
  hgvsp: ENST00000429541.2:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.39G>A
  hgvsp: ENST00000528410.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.27G>A
  hgvsp: ENST00000525502.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.387G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.39G>A
  hgvsp: ENST00000526601.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.121G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.39G>A
  hgvsp: ENST00000343338.7:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.27G>A
  hgvsp: ENST00000526501.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.39G>A
  hgvsp: ENST00000528218.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.27G>A
  hgvsp: ENST00000399602.4:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.72G>A
  hgvsp: ENST00000427810.2:c.72G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.39G>A
  hgvsp: ENST00000534569.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.39G>A
  hgvsp: ENST00000438262.2:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.27G>A
  hgvsp: ENST00000525313.2:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.213G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.39G>A
  hgvsp: ENST00000532539.1:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val9Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

11-3392922-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392922
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392922
    reference: chr 11
allele count: 9
allele frequency: 7.565949862972242e-5
allele num: 118954
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.15G>A
  hgvsp: ENST00000526501.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.27G>A
  hgvsp: ENST00000528410.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.15G>A
  hgvsp: ENST00000399602.4:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.15G>A
  hgvsp: ENST00000530643.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.27G>A
  hgvsp: ENST00000429541.2:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.15G>A
  hgvsp: ENST00000354599.6:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.15G>A
  hgvsp: ENST00000533036.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.27G>A
  hgvsp: ENST00000532539.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.27G>A
  hgvsp: ENST00000528218.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.15G>A
  hgvsp: ENST00000525313.2:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.60G>A
  hgvsp: ENST00000427810.2:c.60G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.27G>A
  hgvsp: ENST00000438262.2:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.27G>A
  hgvsp: ENST00000526601.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.27G>A
  hgvsp: ENST00000529678.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.15G>A
  hgvsp: ENST00000525502.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.27G>A
  hgvsp: ENST00000343338.7:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.15G>A
  hgvsp: ENST00000528796.1:c.15G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.375G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.180G>A
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr5Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

11-3392923-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392923
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392923
    reference: chr 11
allele count: 1
allele frequency: 8.419776370739593e-6
allele num: 118768
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.14C>T
  hgvsp: ENSP00000432720.1:p.Thr5Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.26C>T
  hgvsp: ENSP00000434715.1:p.Thr9Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.14C>T
  hgvsp: ENSP00000005082.9:p.Thr5Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.26C>T
  hgvsp: ENSP00000435153.1:p.Thr9Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.26C>T
  hgvsp: ENSP00000431937.1:p.Thr9Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.26C>T
  hgvsp: ENSP00000387998.2:p.Thr9Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.108C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.14C>T
  hgvsp: ENSP00000435093.1:p.Thr5Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.26C>T
  hgvsp: ENSP00000436384.1:p.Thr9Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.14C>T
  hgvsp: ENSP00000382511.4:p.Thr5Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.200C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.59C>T
  hgvsp: ENSP00000390663.2:p.Thr20Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.14C>T
  hgvsp: ENSP00000433911.1:p.Thr5Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.26C>T
  hgvsp: ENSP00000414353.2:p.Thr9Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.26C>T
  hgvsp: ENSP00000435828.1:p.Thr9Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.374C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.26C>T
  hgvsp: ENSP00000437265.1:p.Thr9Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.14C>T
  hgvsp: ENSP00000434006.1:p.Thr5Met
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.26C>T
  hgvsp: ENSP00000344483.7:p.Thr9Met
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr5Met
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/11-3392943-AAAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392943
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392940
    reference: chr 11
allele count: 113
allele frequency: 9.620460079347511e-4
allele num: 117458
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.16-13_16-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.4-13_4-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.4-13_4-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.49-13_49-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.16-13_16-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.16-13_16-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.4-13_4-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.98-13_98-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.16-13_16-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.190-13_190-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.169-13_169-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.364-13_364-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.16-13_16-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.16-13_16-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.4-13_4-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.4-13_4-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.16-13_16-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.4-13_4-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.16-13_16-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.4-13_4-11delGTT
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.4-13_4-11delGTT
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: AAAC
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

11-3392956-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392956
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392956
    reference: chr 11
allele count: 1
allele frequency: 8.589589417625837e-6
allele num: 116420
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.16-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.4-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.16-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.169-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.4-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.4-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.4-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.16-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.16-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.16-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.4-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.16-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.98-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.4-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.4-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.190-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.16-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.16-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.49-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.4-23T>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.16-23T>A
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

11-3392958-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392958
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392958
    reference: chr 11
allele count: 1
allele frequency: 8.619055006809053e-6
allele num: 116022
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.16-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.364-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.4-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.4-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.98-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.16-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.16-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.4-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.4-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.4-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.49-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.16-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.4-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.190-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.16-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.4-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.16-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.169-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.16-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.4-25G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.4-25G>A
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

11-3392966-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392966
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392966
    reference: chr 11
allele count: 3
allele frequency: 2.620178870877585e-5
allele num: 114496
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.4-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.4-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.49-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.16-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.4-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.4-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.16-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.4-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.4-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.16-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.16-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.98-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.364-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.16-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.16-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.16-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.169-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.16-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.4-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.4-33A>G
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.4-33A>G
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

11-3392971-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392971
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392971
    reference: chr 11
allele count: 1
allele frequency: 8.767776667192733e-6
allele num: 114054
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.16-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.4-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.4-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.4-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.364-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.4-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.4-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.16-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.169-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.4-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.16-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.98-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.4-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.49-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.16-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.4-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.16-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.16-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.16-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.16-38G>A
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.190-38G>A
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

11-3392972-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392972
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392972
    reference: chr 11
allele count: 85122
allele frequency: 7.453243205379658e-1
allele num: 114208
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.16-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.364-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.169-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.4-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.49-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.4-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.4-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.4-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.16-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.16-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.4-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.4-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.16-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.4-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.98-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.4-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.16-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.16-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.16-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.190-39C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.16-39C>T
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 31974
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-3392982-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392982
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392982
    reference: chr 11
allele count: 2
allele frequency: 1.786160825920766e-5
allele num: 111972
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.4-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.4-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.4-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.190-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.16-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.4-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.4-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.169-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.4-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.16-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.16-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.16-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.16-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435153
  ensembl transcript: ENST00000532539
  gene symbol: ZNF195
  hgvsc: ENST00000532539.1:c.16-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.98-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.4-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.364-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.4-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000433911
  ensembl transcript: ENST00000533036
  gene symbol: ZNF195
  hgvsc: ENST00000533036.1:c.4-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.49-49C>T
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.16-49C>T
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-3392985-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 3392985
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 3392985
    reference: chr 11
allele count: 2
allele frequency: 1.79285368521075e-5
allele num: 111554
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000390663
  ensembl transcript: ENST00000427810
  gene symbol: ZNF195
  hgvsc: ENST00000427810.2:c.49-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432720
  ensembl transcript: ENST00000528796
  gene symbol: ZNF195
  hgvsc: ENST00000528796.1:c.4-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000524857
  gene symbol: ZNF195
  hgvsc: ENST00000524857.1:n.169-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000346613
  ensembl transcript: ENST00000354599
  gene symbol: ZNF195
  hgvsc: ENST00000354599.6:c.4-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434715
  ensembl transcript: ENST00000529678
  gene symbol: ZNF195
  hgvsc: ENST00000529678.1:c.16-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435741
  ensembl transcript: ENST00000525313
  gene symbol: ZNF195
  hgvsc: ENST00000525313.2:c.4-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000330692
  gene symbol: ZNF195
  hgvsc: ENST00000330692.7:n.190-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000431937
  ensembl transcript: ENST00000528410
  gene symbol: ZNF195
  hgvsc: ENST00000528410.1:c.16-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000437265
  ensembl transcript: ENST00000534569
  gene symbol: ZNF195
  hgvsc: ENST00000534569.1:c.16-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435828
  ensembl transcript: ENST00000526601
  gene symbol: ZNF195
  hgvsc: ENST00000526601.1:c.16-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000432552
  ensembl transcript: ENST00000526501
  gene symbol: ZNF195
  hgvsc: ENST00000526501.1:c.4-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000435093
  ensembl transcript: ENST00000530643
  gene symbol: ZNF195
  hgvsc: ENST00000530643.1:c.4-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000527386
  gene symbol: ZNF195
  hgvsc: ENST00000527386.1:n.364-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000387998
  ensembl transcript: ENST00000429541
  gene symbol: ZNF195
  hgvsc: ENST00000429541.2:c.16-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000344483
  ensembl transcript: ENST00000343338
  gene symbol: ZNF195
  hgvsc: ENST00000343338.7:c.16-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000414353
  ensembl transcript: ENST00000438262
  gene symbol: ZNF195
  hgvsc: ENST00000438262.2:c.16-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl transcript: ENST00000529085
  gene symbol: ZNF195
  hgvsc: ENST00000529085.1:n.98-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000436384
  ensembl transcript: ENST00000528218
  gene symbol: ZNF195
  hgvsc: ENST00000528218.1:c.16-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000434006
  ensembl transcript: ENST00000525502
  gene symbol: ZNF195
  hgvsc: ENST00000525502.1:c.4-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000005082
  ensembl transcript: ENST00000005082
  gene symbol: ZNF195
  hgvsc: ENST00000005082.9:c.4-52G>C
  variant of: http://identifiers.org/hgnc/12986
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000005801
  ensembl protein: ENSP00000382511
  ensembl transcript: ENST00000399602
  gene symbol: ZNF195
  hgvsc: ENST00000399602.4:c.4-52G>C
  variant of: http://identifiers.org/hgnc/12986
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
num of homozygotes: 0
reference allele: C

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434006
ensembl transcript: ENST00000525502
gene symbol: ZNF195
hgvsc: ENST00000525502.1:c.226+15A>G
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000005082
ensembl transcript: ENST00000005082
gene symbol: ZNF195
hgvsc: ENST00000005082.9:c.226+15A>G
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000390663
ensembl transcript: ENST00000427810
gene symbol: ZNF195
hgvsc: ENST00000427810.2:c.271+15A>G
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 2333
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 767
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1471
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 190
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4912
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3457
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4274
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7629
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8728
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1921
bin: 9.75e1
variant carriers: 5

GenotypeDepth
all individuals: 562
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8094
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 360
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1036
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7791
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6550
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3781
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2028
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2112
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3680
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13913
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3745
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26169
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4844
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
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: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.060089321965083e-4
allele num: 9852
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.64e0

MQRankSum
type: SiteQuality
SIO_000300: 6.850000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.22e0

QD
type: SiteQuality
SIO_000300: 1.239e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
type: SiteQuality
SIO_000300: 2.706736e6

MQ
type: SiteQuality
SIO_000300: 5.944e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.07e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.412+12T>G
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000344483
ensembl transcript: ENST00000343338
gene symbol: ZNF195
hgvsc: ENST00000343338.7:c.238+12T>G
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000436384
ensembl transcript: ENST00000528218
gene symbol: ZNF195
hgvsc: ENST00000528218.1:c.238+12T>G
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 1471
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 562
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 184
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 8.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2334
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8110
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1916
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 67
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6552
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7628
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8736
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4271
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3458
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 360
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4912
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 767
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7791
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1036
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26167
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4844
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3780
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3680
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2027
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2109
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3746
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13936
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9854
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.469010175763182e-4
allele num: 8648
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: 16496
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.70646e6

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

QD
type: SiteQuality
SIO_000300: 1.39e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000529085
gene symbol: ZNF195
hgvsc: ENST00000529085.1:n.320+9G>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000346613
ensembl transcript: ENST00000354599
gene symbol: ZNF195
hgvsc: ENST00000354599.6:c.226+9G>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.412+9G>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000344483
ensembl transcript: ENST00000343338
gene symbol: ZNF195
hgvsc: ENST00000343338.7:c.238+9G>C
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 1913
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 427
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7633
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4274
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4913
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2334
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3458
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7795
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 186
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8739
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 360
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1036
bin: 7.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 767
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 6551
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8113
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 562
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1471
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13959
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4834
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 3785
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2106
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2028
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26165
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3679
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3745
bin: 8.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9854
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: -5.127e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.577e0

FS
type: SiteQuality
SIO_000300: 1.648e0

DP
type: SiteQuality
SIO_000300: 2.706019e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.99e-1

QD
type: SiteQuality
SIO_000300: 1.195e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000346613
ensembl transcript: ENST00000354599
gene symbol: ZNF195
hgvsc: ENST00000354599.6:c.226+3G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000387998
ensembl transcript: ENST00000429541
gene symbol: ZNF195
hgvsc: ENST00000429541.2:c.238+3G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000524857
gene symbol: ZNF195
hgvsc: ENST00000524857.1:n.391+3G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435153
ensembl transcript: ENST00000532539
gene symbol: ZNF195
hgvsc: ENST00000532539.1:c.238+3G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000529789
gene symbol: ZNF195
hgvsc: ENST00000529789.1:n.173+3G>A
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 1912
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 767
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2334
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1036
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7797
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8741
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4913
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3458
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 562
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 185
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1471
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7629
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 360
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4269
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6552
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8140
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3742
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13996
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4841
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3679
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2110
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3777
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26166
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2029
bin: 8.75e1
variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9858
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211680600993578e-4
allele num: 16506
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.186e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.453e0

DP
type: SiteQuality
SIO_000300: 2.706489e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e0

VQSLOD
type: SiteQuality
SIO_000300: 5.06e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -8.34e-1

QD
type: SiteQuality
SIO_000300: 1.182e1

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435741
ensembl transcript: ENST00000525313
gene symbol: ZNF195
hgvsc: ENST00000525313.2:c.225A>G
hgvsp: ENST00000525313.2:c.225A>G(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000529789
gene symbol: ZNF195
hgvsc: ENST00000529789.1:n.172A>G
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
consequence: splice_region_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000005082
ensembl transcript: ENST00000005082
gene symbol: ZNF195
hgvsc: ENST00000005082.9:c.225A>G
hgvsp: ENST00000005082.9:c.225A>G(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000436384
ensembl transcript: ENST00000528218
gene symbol: ZNF195
hgvsc: ENST00000528218.1:c.237A>G
hgvsp: ENST00000528218.1:c.237A>G(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
consequence: splice_region_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.411A>G
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: true
consequence: synonymous_variant
consequence: splice_region_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000382511
ensembl transcript: ENST00000399602
gene symbol: ZNF195
hgvsc: ENST00000399602.4:c.225A>G
hgvsp: ENST00000399602.4:c.225A>G(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
consequence: splice_region_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000431937
ensembl transcript: ENST00000528410
gene symbol: ZNF195
hgvsc: ENST00000528410.1:c.237A>G
hgvsp: ENST00000528410.1:c.237A>G(p.%3D)
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 23
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 182
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4913
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4273
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7795
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 767
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7629
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1913
bin: 9.75e1
variant carriers: 14

GenotypeDepth
all individuals: 3458
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6552
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8144
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1036
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1471
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 562
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8745
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 358
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2334
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14006
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2029
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2112
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26164
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3741
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3679
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4844
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3780
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
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: 16506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9858
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 13
allele frequency: 1.965527668581796e-3
allele num: 6614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49907057624273e-5
allele num: 66708
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.361e1

MQRankSum
type: SiteQuality
SIO_000300: -1.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.95e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.76e-1

FS
type: SiteQuality
SIO_000300: 5.38e-1

DP
type: SiteQuality
SIO_000300: 2.707911e6

VQSLOD
type: SiteQuality
SIO_000300: 1.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.6e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434006
ensembl transcript: ENST00000525502
gene symbol: ZNF195
hgvsc: ENST00000525502.1:c.220C>T
hgvsp: ENSP00000434006.1:p.His74Tyr
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000524857
gene symbol: ZNF195
hgvsc: ENST00000524857.1:n.385C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000527386
gene symbol: ZNF195
hgvsc: ENST00000527386.1:n.580C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000529789
gene symbol: ZNF195
hgvsc: ENST00000529789.1:n.167C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000387998
ensembl transcript: ENST00000429541
gene symbol: ZNF195
hgvsc: ENST00000429541.2:c.232C>T
hgvsp: ENSP00000387998.2:p.His78Tyr
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000344483
ensembl transcript: ENST00000343338
gene symbol: ZNF195
hgvsc: ENST00000343338.7:c.232C>T
hgvsp: ENSP00000344483.7:p.His78Tyr
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 8747
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4275
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1900
bin: 9.75e1
variant carriers: 2

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

GenotypeDepth
all individuals: 1472
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7635
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6555
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4914
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 7795
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8145
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1036
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 187
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2334
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3458
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 358
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 562
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3742
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4846
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3681
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14020
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26158
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 3780
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2112
bin: 7.25e1
variant carriers: 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: 16510
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9860
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.998141152485459e-5
allele num: 66708
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: 11578
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQRankSum
type: SiteQuality
SIO_000300: 2.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.648e0

VQSLOD
type: SiteQuality
SIO_000300: 3.34e0

QD
type: SiteQuality
SIO_000300: 1.233e1

MQ
type: SiteQuality
SIO_000300: 5.951e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 2.707249e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.57e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000344483
ensembl transcript: ENST00000343338
gene symbol: ZNF195
hgvsc: ENST00000343338.7:c.232C>A
hgvsp: ENSP00000344483.7:p.His78Asn
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000432552
ensembl transcript: ENST00000526501
gene symbol: ZNF195
hgvsc: ENST00000526501.1:c.220C>A
hgvsp: ENSP00000432552.1:p.His74Asn
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000346613
ensembl transcript: ENST00000354599
gene symbol: ZNF195
hgvsc: ENST00000354599.6:c.220C>A
hgvsp: ENSP00000346613.6:p.His74Asn
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435741
ensembl transcript: ENST00000525313
gene symbol: ZNF195
hgvsc: ENST00000525313.2:c.220C>A
hgvsp: ENSP00000435741.1:p.His74Asn
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000529789
gene symbol: ZNF195
hgvsc: ENST00000529789.1:n.167C>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000432720
ensembl transcript: ENST00000528796
gene symbol: ZNF195
hgvsc: ENST00000528796.1:c.220C>A
hgvsp: ENSP00000432720.1:p.His74Asn
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 768
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4275
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 7635
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 427
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6555
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8145
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1472
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3458
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1036
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 562
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 187
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7795
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8747
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1900
bin: 9.75e1
variant carriers: 12

GenotypeDepth
all individuals: 2334
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 358
bin: 9.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4914
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3780
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14020
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4846
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26158
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2112
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3681
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3742
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
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: 16510
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 1.217038539553753e-3
allele num: 9860
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: 8648
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.707249e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.648e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.34e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.57e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.26e-1

QD
type: SiteQuality
SIO_000300: 1.233e1

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000382511
ensembl transcript: ENST00000399602
gene symbol: ZNF195
hgvsc: ENST00000399602.4:c.217G>A
hgvsp: ENSP00000382511.4:p.Gly73Arg
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000344483
ensembl transcript: ENST00000343338
gene symbol: ZNF195
hgvsc: ENST00000343338.7:c.229G>A
hgvsp: ENSP00000344483.7:p.Gly77Arg
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435153
ensembl transcript: ENST00000532539
gene symbol: ZNF195
hgvsc: ENST00000532539.1:c.229G>A
hgvsp: ENSP00000435153.1:p.Gly77Arg
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434006
ensembl transcript: ENST00000525502
gene symbol: ZNF195
hgvsc: ENST00000525502.1:c.217G>A
hgvsp: ENSP00000434006.1:p.Gly73Arg
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000433911
ensembl transcript: ENST00000533036
gene symbol: ZNF195
hgvsc: ENST00000533036.1:c.217G>A
hgvsp: ENSP00000433911.1:p.Gly73Arg
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.403G>A
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 562
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1473
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1889
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 4917
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 426
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7798
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2336
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8749
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 190
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1036
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6555
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 358
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7637
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3458
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8151
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4267
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2112
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26155
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3681
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4849
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3743
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3781
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14009
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997961386257345e-5
allele num: 66712
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: 11578
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: 8648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.958e1

VQSLOD
type: SiteQuality
SIO_000300: 7.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 2.703948e6

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.66e-1

QD
type: SiteQuality
SIO_000300: 1.173e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.55e0

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000414353
ensembl transcript: ENST00000438262
gene symbol: ZNF195
hgvsc: ENST00000438262.2:c.228C>T
hgvsp: ENST00000438262.2:c.228C>T(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000432720
ensembl transcript: ENST00000528796
gene symbol: ZNF195
hgvsc: ENST00000528796.1:c.216C>T
hgvsp: ENST00000528796.1:c.216C>T(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434361
ensembl transcript: ENST00000529228
gene symbol: ZNF195
hgvsc: ENST00000529228.1:c.87C>T
hgvsp: ENST00000529228.1:c.87C>T(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.402C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000529789
gene symbol: ZNF195
hgvsc: ENST00000529789.1:n.163C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000436384
ensembl transcript: ENST00000528218
gene symbol: ZNF195
hgvsc: ENST00000528218.1:c.228C>T
hgvsp: ENST00000528218.1:c.228C>T(p.%3D)
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 426
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6556
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8750
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 188
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 358
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3458
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8154
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 561
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1034
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2336
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4268
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 47
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4917
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1890
bin: 9.75e1
variant carriers: 11

GenotypeDepth
all individuals: 7798
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7637
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 769
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1473
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3781
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4847
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2112
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3683
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3743
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14016
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26155
bin: 9.75e1
variant carriers: 12

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: 16510
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9860
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

East Asian
type: Population
allele count: 12
allele frequency: 1.387604070305273e-3
allele num: 8648
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

QD
type: SiteQuality
SIO_000300: 1.157e1

VQSLOD
type: SiteQuality
SIO_000300: 6.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.86e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.3e-2

DP
type: SiteQuality
SIO_000300: 2.705258e6

MQ
type: SiteQuality
SIO_000300: 5.945e1

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000432552
ensembl transcript: ENST00000526501
gene symbol: ZNF195
hgvsc: ENST00000526501.1:c.207G>A
hgvsp: ENST00000526501.1:c.207G>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000437265
ensembl transcript: ENST00000534569
gene symbol: ZNF195
hgvsc: ENST00000534569.1:c.219G>A
hgvsp: ENST00000534569.1:c.219G>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000346613
ensembl transcript: ENST00000354599
gene symbol: ZNF195
hgvsc: ENST00000354599.6:c.207G>A
hgvsp: ENST00000354599.6:c.207G>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.393G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000524857
gene symbol: ZNF195
hgvsc: ENST00000524857.1:n.372G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000527386
gene symbol: ZNF195
hgvsc: ENST00000527386.1:n.567G>A
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 1034
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4274
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7639
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8754
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1473
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 561
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6556
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2336
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1879
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 185
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8158
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 426
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3458
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7800
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4917
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 358
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3684
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2111
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14028
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3780
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3747
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4850
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26144
bin: 9.75e1
variant carriers: 2

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.01440454453236e-4
allele num: 9858
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
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: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.25e0

MQRankSum
type: SiteQuality
SIO_000300: 2.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.524e0

MQ
type: SiteQuality
SIO_000300: 5.904e1

VQSLOD
type: SiteQuality
SIO_000300: -1.976e-1

DP
type: SiteQuality
SIO_000300: 2.703251e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.622e0

QD
type: SiteQuality
SIO_000300: 1.117e1

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435741
ensembl transcript: ENST00000525313
gene symbol: ZNF195
hgvsc: ENST00000525313.2:c.204G>A
hgvsp: ENST00000525313.2:c.204G>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000527386
gene symbol: ZNF195
hgvsc: ENST00000527386.1:n.564G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000433911
ensembl transcript: ENST00000533036
gene symbol: ZNF195
hgvsc: ENST00000533036.1:c.204G>A
hgvsp: ENST00000533036.1:c.204G>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000524857
gene symbol: ZNF195
hgvsc: ENST00000524857.1:n.369G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000390663
ensembl transcript: ENST00000427810
gene symbol: ZNF195
hgvsc: ENST00000427810.2:c.249G>A
hgvsp: ENST00000427810.2:c.249G>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434361
ensembl transcript: ENST00000529228
gene symbol: ZNF195
hgvsc: ENST00000529228.1:c.75G>A
hgvsp: ENST00000529228.1:c.75G>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 7639
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 561
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8755
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1473
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 54
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1877
bin: 9.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 4276
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8160
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 184
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1034
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6556
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2336
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 358
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 426
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4917
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7801
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3459
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4853
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14031
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3684
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3747
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26143
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3780
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2030
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2112
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 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: 16510
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.01440454453236e-4
allele num: 9858
num of homozygotes: 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: 8648
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.7e-2

FS
type: SiteQuality
SIO_000300: 2.636e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.582e0

DP
type: SiteQuality
SIO_000300: 2.702945e6

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.273e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.9e-2

QD
type: SiteQuality
SIO_000300: 1.212e1

VQSLOD
type: SiteQuality
SIO_000300: 3.69e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000527386
gene symbol: ZNF195
hgvsc: ENST00000527386.1:n.557A>G
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000432552
ensembl transcript: ENST00000526501
gene symbol: ZNF195
hgvsc: ENST00000526501.1:c.197A>G
hgvsp: ENSP00000432552.1:p.Lys66Arg
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.383A>G
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000382511
ensembl transcript: ENST00000399602
gene symbol: ZNF195
hgvsc: ENST00000399602.4:c.197A>G
hgvsp: ENSP00000382511.4:p.Lys66Arg
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000529789
gene symbol: ZNF195
hgvsc: ENST00000529789.1:n.144A>G
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000436384
ensembl transcript: ENST00000528218
gene symbol: ZNF195
hgvsc: ENST00000528218.1:c.209A>G
hgvsp: ENSP00000436384.1:p.Lys70Arg
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 2336
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 426
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1034
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4917
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4273
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1876
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 8166
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7640
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 6556
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8754
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3459
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 358
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1473
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 561
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7801
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3747
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2112
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14041
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3780
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26142
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3685
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4853
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2030
bin: 8.75e1
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: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9858
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: 904
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.99e-1

QD
type: SiteQuality
SIO_000300: 1.374e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-1

FS
type: SiteQuality
SIO_000300: 3.277e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

MQRankSum
type: SiteQuality
SIO_000300: 7.57e-1

DP
type: SiteQuality
SIO_000300: 2.703087e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.91e0

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000432552
ensembl transcript: ENST00000526501
gene symbol: ZNF195
hgvsc: ENST00000526501.1:c.176G>A
hgvsp: ENSP00000432552.1:p.Arg59Gln
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434715
ensembl transcript: ENST00000529678
gene symbol: ZNF195
hgvsc: ENST00000529678.1:c.188G>A
hgvsp: ENSP00000434715.1:p.Arg63Gln
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000344483
ensembl transcript: ENST00000343338
gene symbol: ZNF195
hgvsc: ENST00000343338.7:c.188G>A
hgvsp: ENSP00000344483.7:p.Arg63Gln
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000527386
gene symbol: ZNF195
hgvsc: ENST00000527386.1:n.536G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000382511
ensembl transcript: ENST00000399602
gene symbol: ZNF195
hgvsc: ENST00000399602.4:c.176G>A
hgvsp: ENSP00000382511.4:p.Arg59Gln
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434006
ensembl transcript: ENST00000525502
gene symbol: ZNF195
hgvsc: ENST00000525502.1:c.176G>A
hgvsp: ENSP00000434006.1:p.Arg59Gln
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 8177
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8754
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4246
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2336
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3460
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 426
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7642
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4918
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1033
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 561
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1876
bin: 9.75e1
variant carriers: 5

GenotypeDepth
all individuals: 6556
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1474
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7800
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3685
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3746
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2107
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14029
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4857
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26143
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 3780
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.422774076317383e-4
allele num: 16510
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9854
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.997422216893472e-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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e0

DP
type: SiteQuality
SIO_000300: 2.703078e6

MQ
type: SiteQuality
SIO_000300: 5.932e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.39e-1

QD
type: SiteQuality
SIO_000300: 1.281e1

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435093
ensembl transcript: ENST00000530643
gene symbol: ZNF195
hgvsc: ENST00000530643.1:c.175C>A
hgvsp: ENST00000530643.1:c.175C>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000387998
ensembl transcript: ENST00000429541
gene symbol: ZNF195
hgvsc: ENST00000429541.2:c.187C>A
hgvsp: ENST00000429541.2:c.187C>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000432720
ensembl transcript: ENST00000528796
gene symbol: ZNF195
hgvsc: ENST00000528796.1:c.175C>A
hgvsp: ENST00000528796.1:c.175C>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000437265
ensembl transcript: ENST00000534569
gene symbol: ZNF195
hgvsc: ENST00000534569.1:c.187C>A
hgvsp: ENST00000534569.1:c.187C>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000382511
ensembl transcript: ENST00000399602
gene symbol: ZNF195
hgvsc: ENST00000399602.4:c.175C>A
hgvsp: ENST00000399602.4:c.175C>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435741
ensembl transcript: ENST00000525313
gene symbol: ZNF195
hgvsc: ENST00000525313.2:c.175C>A
hgvsp: ENST00000525313.2:c.175C>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 1474
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4241
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7800
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 170
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2336
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 7641
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8180
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 426
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1872
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 561
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3460
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4920
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1033
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8755
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6557
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3780
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2107
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14023
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3685
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26139
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4856
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3746
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9854
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: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 2.863e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.11e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

QD
type: SiteQuality
SIO_000300: 1.249e1

DP
type: SiteQuality
SIO_000300: 2.702282e6

MQ
type: SiteQuality
SIO_000300: 5.977e1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000346613
ensembl transcript: ENST00000354599
gene symbol: ZNF195
hgvsc: ENST00000354599.6:c.165C>T
hgvsp: ENST00000354599.6:c.165C>T(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.351C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434715
ensembl transcript: ENST00000529678
gene symbol: ZNF195
hgvsc: ENST00000529678.1:c.177C>T
hgvsp: ENST00000529678.1:c.177C>T(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000529085
gene symbol: ZNF195
hgvsc: ENST00000529085.1:n.259C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000432720
ensembl transcript: ENST00000528796
gene symbol: ZNF195
hgvsc: ENST00000528796.1:c.165C>T
hgvsp: ENST00000528796.1:c.165C>T(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000527386
gene symbol: ZNF195
hgvsc: ENST00000527386.1:n.525C>T
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 7643
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8756
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1033
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 562
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 159
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 3459
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1871
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 425
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7800
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8184
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1474
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4219
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4918
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2337
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 58
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6557
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2105
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14020
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 8.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 3685
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4854
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 70
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26138
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3775
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3746
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
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: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9852
num of homozygotes: 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: 11576
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.209e0

DP
type: SiteQuality
SIO_000300: 2.701913e6

MQ
type: SiteQuality
SIO_000300: 5.966e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

QD
type: SiteQuality
SIO_000300: 1.261e1

VQSLOD
type: SiteQuality
SIO_000300: 3.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.417e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.78e-1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000432720
ensembl transcript: ENST00000528796
gene symbol: ZNF195
hgvsc: ENST00000528796.1:c.158T>C
hgvsp: ENSP00000432720.1:p.Ile53Thr
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000433911
ensembl transcript: ENST00000533036
gene symbol: ZNF195
hgvsc: ENST00000533036.1:c.158T>C
hgvsp: ENSP00000433911.1:p.Ile53Thr
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435093
ensembl transcript: ENST00000530643
gene symbol: ZNF195
hgvsc: ENST00000530643.1:c.158T>C
hgvsp: ENSP00000435093.1:p.Ile53Thr
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000382511
ensembl transcript: ENST00000399602
gene symbol: ZNF195
hgvsc: ENST00000399602.4:c.158T>C
hgvsp: ENSP00000382511.4:p.Ile53Thr
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434715
ensembl transcript: ENST00000529678
gene symbol: ZNF195
hgvsc: ENST00000529678.1:c.170T>C
hgvsp: ENSP00000434715.1:p.Ile57Thr
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000346613
ensembl transcript: ENST00000354599
gene symbol: ZNF195
hgvsc: ENST00000354599.6:c.158T>C
hgvsp: ENSP00000346613.6:p.Ile53Thr
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 561
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4210
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8172
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7642
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1474
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 9.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1870
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8757
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6557
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 155
bin: 2.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 1033
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3459
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 425
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4919
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7801
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2336
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2101
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3747
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14006
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4844
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26136
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3685
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3774
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 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: 9850
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
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: 11572
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.91e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.73e-1

QD
type: SiteQuality
SIO_000300: 1.162e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.4e-2

FS
type: SiteQuality
SIO_000300: 2.752e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.52e0

DP
type: SiteQuality
SIO_000300: 2.701399e6

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434006
ensembl transcript: ENST00000525502
gene symbol: ZNF195
hgvsc: ENST00000525502.1:c.148C>T
hgvsp: ENSP00000434006.1:p.Pro50Ser
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000529789
gene symbol: ZNF195
hgvsc: ENST00000529789.1:n.95C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000437265
ensembl transcript: ENST00000534569
gene symbol: ZNF195
hgvsc: ENST00000534569.1:c.160C>T
hgvsp: ENSP00000437265.1:p.Pro54Ser
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000527386
gene symbol: ZNF195
hgvsc: ENST00000527386.1:n.508C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434361
ensembl transcript: ENST00000529228
gene symbol: ZNF195
hgvsc: ENST00000529228.1:c.19C>T
hgvsp: ENSP00000434361.1:p.Pro7Ser
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000414353
ensembl transcript: ENST00000438262
gene symbol: ZNF195
hgvsc: ENST00000438262.2:c.160C>T
hgvsp: ENSP00000414353.2:p.Pro54Ser
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 356
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1869
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1033
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7799
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 767
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 562
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4154
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8757
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7640
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 8163
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1474
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 425
bin: 8.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4918
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 67
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6558
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2336
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3460
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4826
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2029
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 155
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13944
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2095
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3770
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3744
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3685
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26135
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9848
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: 0
allele frequency: 0.0e0
allele num: 8644
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: -2.83e0

QD
type: SiteQuality
SIO_000300: 4.08e0

MQRankSum
type: SiteQuality
SIO_000300: -2.138e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.43e-1

DP
type: SiteQuality
SIO_000300: 2.700342e6

FS
type: SiteQuality
SIO_000300: 6.955e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.610000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.483e0

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000437265
ensembl transcript: ENST00000534569
gene symbol: ZNF195
hgvsc: ENST00000534569.1:c.155G>T
hgvsp: ENSP00000437265.1:p.Cys52Phe
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435741
ensembl transcript: ENST00000525313
gene symbol: ZNF195
hgvsc: ENST00000525313.2:c.143G>T
hgvsp: ENSP00000435741.1:p.Cys48Phe
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000527386
gene symbol: ZNF195
hgvsc: ENST00000527386.1:n.503G>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000529789
gene symbol: ZNF195
hgvsc: ENST00000529789.1:n.90G>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434715
ensembl transcript: ENST00000529678
gene symbol: ZNF195
hgvsc: ENST00000529678.1:c.155G>T
hgvsp: ENSP00000434715.1:p.Cys52Phe
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435153
ensembl transcript: ENST00000532539
gene symbol: ZNF195
hgvsc: ENST00000532539.1:c.155G>T
hgvsp: ENSP00000435153.1:p.Cys52Phe
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 7641
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6560
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1868
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1475
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8137
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8743
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 149
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7801
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 140
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 80
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4920
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 562
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1033
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2335
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 425
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4093
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3459
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 767
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3686
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2091
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 153
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13864
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4808
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3767
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3742
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2029
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26134
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16484
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
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.97e-1

FS
type: SiteQuality
SIO_000300: 2.45e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.395e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.423e1

MQ
type: SiteQuality
SIO_000300: 5.957e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

DP
type: SiteQuality
SIO_000300: 2.699088e6

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000382511
ensembl transcript: ENST00000399602
gene symbol: ZNF195
hgvsc: ENST00000399602.4:c.139G>C
hgvsp: ENSP00000382511.4:p.Val47Leu
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000344483
ensembl transcript: ENST00000343338
gene symbol: ZNF195
hgvsc: ENST00000343338.7:c.151G>C
hgvsp: ENSP00000344483.7:p.Val51Leu
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000432552
ensembl transcript: ENST00000526501
gene symbol: ZNF195
hgvsc: ENST00000526501.1:c.139G>C
hgvsp: ENSP00000432552.1:p.Val47Leu
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000529085
gene symbol: ZNF195
hgvsc: ENST00000529085.1:n.233G>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000390663
ensembl transcript: ENST00000427810
gene symbol: ZNF195
hgvsc: ENST00000427810.2:c.184G>C
hgvsp: ENSP00000390663.2:p.Val62Leu
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434006
ensembl transcript: ENST00000525502
gene symbol: ZNF195
hgvsc: ENST00000525502.1:c.139G>C
hgvsp: ENSP00000434006.1:p.Val47Leu
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 424
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1475
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8122
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4039
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7641
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 195
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 132
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6563
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3459
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 48
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4918
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 767
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2335
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1034
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8738
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7803
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 561
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1868
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2088
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4798
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3685
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13797
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26134
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 3739
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3768
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2028
bin: 8.75e1
variant carriers: 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
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
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: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9826
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.331e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.98e-1

FS
type: SiteQuality
SIO_000300: 1.1889e1

MQRankSum
type: SiteQuality
SIO_000300: 6.01e-1

DP
type: SiteQuality
SIO_000300: 2.698087e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.251e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.514e1

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434715
ensembl transcript: ENST00000529678
gene symbol: ZNF195
hgvsc: ENST00000529678.1:c.143-4A>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.317-4A>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435741
ensembl transcript: ENST00000525313
gene symbol: ZNF195
hgvsc: ENST00000525313.2:c.131-4A>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000431937
ensembl transcript: ENST00000528410
gene symbol: ZNF195
hgvsc: ENST00000528410.1:c.143-4A>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000390663
ensembl transcript: ENST00000427810
gene symbol: ZNF195
hgvsc: ENST00000427810.2:c.176-4A>T
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 158
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7631
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8648
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1034
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1867
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 561
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7783
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 638
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2335
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3714
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3458
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6557
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 767
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7903
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1474
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4918
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 424
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3738
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3681
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 182
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2025
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2069
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13146
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26131
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 530
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3760
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4717
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66558
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9802
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.528e1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.334e0

FS
type: SiteQuality
SIO_000300: 2.051e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e-2

DP
type: SiteQuality
SIO_000300: 2.688407e6

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000414353
ensembl transcript: ENST00000438262
gene symbol: ZNF195
hgvsc: ENST00000438262.2:c.143-6A>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000431937
ensembl transcript: ENST00000528410
gene symbol: ZNF195
hgvsc: ENST00000528410.1:c.143-6A>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.317-6A>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000436384
ensembl transcript: ENST00000528218
gene symbol: ZNF195
hgvsc: ENST00000528218.1:c.143-6A>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434006
ensembl transcript: ENST00000525502
gene symbol: ZNF195
hgvsc: ENST00000525502.1:c.131-6A>C
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 4918
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 712
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3458
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 210
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 561
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3666
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 424
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7630
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6558
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7860
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7772
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2335
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1866
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1474
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 200
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1034
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 356
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8623
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 767
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3759
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3738
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2024
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 586
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2072
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4708
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26132
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 13020
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3681
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66554
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.114711997064938e-5
allele num: 16354
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
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: 900
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.32e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.64e0

VQSLOD
type: SiteQuality
SIO_000300: -1.217e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.686592e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.355e1

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000432720
ensembl transcript: ENST00000528796
gene symbol: ZNF195
hgvsc: ENST00000528796.1:c.131-7A>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435741
ensembl transcript: ENST00000525313
gene symbol: ZNF195
hgvsc: ENST00000525313.2:c.131-7A>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000437265
ensembl transcript: ENST00000534569
gene symbol: ZNF195
hgvsc: ENST00000534569.1:c.143-7A>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000433911
ensembl transcript: ENST00000533036
gene symbol: ZNF195
hgvsc: ENST00000533036.1:c.131-7A>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000524857
gene symbol: ZNF195
hgvsc: ENST00000524857.1:n.296-7A>C
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 2335
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7772
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3458
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 425
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1474
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7823
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 213
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 216
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1866
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 768
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 106
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 759
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1034
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4918
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7629
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 355
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6558
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3654
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 560
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8606
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2023
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2072
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3739
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4707
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26131
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 37
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3759
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3682
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12978
bin: 6.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66546
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.729804532087874e-4
allele num: 11562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16356
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.24e-1

QD
type: SiteQuality
SIO_000300: 1.627e1

DP
type: SiteQuality
SIO_000300: 2.685632e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.19e0

FS
type: SiteQuality
SIO_000300: 3.507e0

MQ
type: SiteQuality
SIO_000300: 5.924e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -6.3e-2

Annotation
canonical: true
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000382511
ensembl transcript: ENST00000399602
gene symbol: ZNF195
hgvsc: ENST00000399602.4:c.131-8T>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435741
ensembl transcript: ENST00000525313
gene symbol: ZNF195
hgvsc: ENST00000525313.2:c.131-8T>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434006
ensembl transcript: ENST00000525502
gene symbol: ZNF195
hgvsc: ENST00000525502.1:c.131-8T>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.317-8T>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435153
ensembl transcript: ENST00000532539
gene symbol: ZNF195
hgvsc: ENST00000532539.1:c.143-8T>C
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 1866
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7627
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3458
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6557
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2335
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3584
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 263
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7770
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 355
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 560
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8599
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 107
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7760
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 841
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1474
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 424
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1034
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 767
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4918
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12785
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3757
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3739
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3681
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2069
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26130
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2023
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 676
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4695
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
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: 1.503036132988637e-5
allele num: 66532
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.86e-1

DP
type: SiteQuality
SIO_000300: 2.683718e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

VQSLOD
type: SiteQuality
SIO_000300: 4.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.56e-1

QD
type: SiteQuality
SIO_000300: 2.171e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.28e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000529085
gene symbol: ZNF195
hgvsc: ENST00000529085.1:n.225-13T>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000527386
gene symbol: ZNF195
hgvsc: ENST00000527386.1:n.491-13T>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000344483
ensembl transcript: ENST00000343338
gene symbol: ZNF195
hgvsc: ENST00000343338.7:c.143-13T>C
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 2335
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7592
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 104
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6553
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 357
bin: 9.25e1
variant carriers: 3

GenotypeDepth
all individuals: 3395
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1090
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7757
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1035
bin: 7.25e1
variant carriers: 3

GenotypeDepth
all individuals: 425
bin: 8.75e1
variant carriers: 2

GenotypeDepth
all individuals: 8559
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 558
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 270
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 767
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 387
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7625
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1864
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 4919
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3458
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1474
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2055
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3751
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4637
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 356
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12462
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26129
bin: 9.75e1
variant carriers: 12

GenotypeQuality
all individuals: 87
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3681
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2022
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3727
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66494
num of homozygotes: 0

African
type: Population
allele count: 11
allele frequency: 1.123136614253625e-3
allele num: 9794
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.653513326410523e-5
allele num: 11556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16304
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.977e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.5e0

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.23e0

DP
type: SiteQuality
SIO_000300: 2.678428e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.601e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000005082
ensembl transcript: ENST00000005082
gene symbol: ZNF195
hgvsc: ENST00000005082.9:c.131-18T>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.317-18T>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000437265
ensembl transcript: ENST00000534569
gene symbol: ZNF195
hgvsc: ENST00000534569.1:c.143-18T>C
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 626
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 558
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6552
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 355
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3098
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1030
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8498
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7326
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 92
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1451
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1475
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7622
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 309
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7748
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4920
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3459
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2334
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1863
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 423
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 766
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1065
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4561
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11873
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 501
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2053
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2021
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3748
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3728
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3681
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26117
bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66454
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.144770800049158e-5
allele num: 16274
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.97e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.0e0

QD
type: SiteQuality
SIO_000300: 1.491e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.336e0

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.02e-1

DP
type: SiteQuality
SIO_000300: 2.669998e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000431937
ensembl transcript: ENST00000528410
gene symbol: ZNF195
hgvsc: ENST00000528410.1:c.143-31A>G
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434715
ensembl transcript: ENST00000529678
gene symbol: ZNF195
hgvsc: ENST00000529678.1:c.143-31A>G
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435153
ensembl transcript: ENST00000532539
gene symbol: ZNF195
hgvsc: ENST00000532539.1:c.143-31A>G
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 3459
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7881
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6542
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2442
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 355
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7613
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 425
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2239
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6183
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 765
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 423
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2295
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 556
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 99
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1031
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 2334
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1862
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1473
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4916
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7592
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3667
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3698
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4250
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 891
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26105
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 266
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1698
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3718
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9356
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2017
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.328830926874709e-4
allele num: 8588
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66302
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16140
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.634984e6

MQ
type: SiteQuality
SIO_000300: 5.873e1

QD
type: SiteQuality
SIO_000300: 1.654e1

MQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

VQSLOD
type: SiteQuality
SIO_000300: -1.016e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -6.57e-1

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000436384
ensembl transcript: ENST00000528218
gene symbol: ZNF195
hgvsc: ENST00000528218.1:c.143-47T>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000414353
ensembl transcript: ENST00000438262
gene symbol: ZNF195
hgvsc: ENST00000438262.2:c.143-47T>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000344483
ensembl transcript: ENST00000343338
gene symbol: ZNF195
hgvsc: ENST00000343338.7:c.143-47T>C
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 765
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2475
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2330
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3583
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1472
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4720
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6450
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6522
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 423
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3451
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 680
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4919
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 3875
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1862
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7376
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1029
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 355
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7533
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 556
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1518
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1863
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 977
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1742
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2006
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3583
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1560
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3686
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26081
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 171
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1847
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3395
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4800
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3648
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1870
bin: 4.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15882
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9710
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.516990291262136e-5
allele num: 65920
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.006e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.59e-1

DP
type: SiteQuality
SIO_000300: 2.596561e6

MQ
type: SiteQuality
SIO_000300: 5.721e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.33e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.142e0

QD
type: SiteQuality
SIO_000300: 1.447e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 9.89e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000433911
ensembl transcript: ENST00000533036
gene symbol: ZNF195
hgvsc: ENST00000533036.1:c.131-51A>G
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.317-51A>G
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000390663
ensembl transcript: ENST00000427810
gene symbol: ZNF195
hgvsc: ENST00000427810.2:c.176-51A>G
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 6319
bin: 4.75e1
variant carriers: 5895

GenotypeDepth
all individuals: 4137
bin: 2.25e1
variant carriers: 3802

GenotypeDepth
all individuals: 6782
bin: 3.25e1
variant carriers: 6285

GenotypeDepth
all individuals: 3146
bin: 5.75e1
variant carriers: 2966

GenotypeDepth
all individuals: 1345
bin: 6.75e1
variant carriers: 1273

GenotypeDepth
all individuals: 904
bin: 7.25e1
variant carriers: 853

GenotypeDepth
all individuals: 1999
bin: 6.25e1
variant carriers: 1851

GenotypeDepth
all individuals: 767
bin: 7.5e0
variant carriers: 655

GenotypeDepth
all individuals: 2595
bin: 1.25e1
variant carriers: 2346

GenotypeDepth
all individuals: 4570
bin: 5.25e1
variant carriers: 4286

GenotypeDepth
all individuals: 362
bin: 9.25e1
variant carriers: 344

GenotypeDepth
all individuals: 69
bin: 2.5e0
variant carriers: 35

GenotypeDepth
all individuals: 5157
bin: 2.75e1
variant carriers: 4770

GenotypeDepth
all individuals: 3745
bin: 1.75e1
variant carriers: 3418

GenotypeDepth
all individuals: 414
bin: 8.75e1
variant carriers: 396

GenotypeDepth
all individuals: 695
bin: 7.75e1
variant carriers: 654

GenotypeDepth
all individuals: 7684
bin: 3.75e1
variant carriers: 7126

GenotypeDepth
all individuals: 7545
bin: 4.25e1
variant carriers: 7057

GenotypeDepth
all individuals: 1695
bin: 9.75e1
variant carriers: 1605

GenotypeDepth
all individuals: 512
bin: 8.25e1
variant carriers: 480

GenotypeQuality
all individuals: 561
bin: 5.75e1
variant carriers: 497

GenotypeQuality
all individuals: 122
bin: 7.5e0
variant carriers: 79

GenotypeQuality
all individuals: 777
bin: 3.75e1
variant carriers: 601

GenotypeQuality
all individuals: 950
bin: 4.75e1
variant carriers: 778

GenotypeQuality
all individuals: 1158
bin: 6.75e1
variant carriers: 929

GenotypeQuality
all individuals: 495
bin: 4.25e1
variant carriers: 396

GenotypeQuality
all individuals: 46999
bin: 9.75e1
variant carriers: 45480

GenotypeQuality
all individuals: 628
bin: 3.25e1
variant carriers: 475

GenotypeQuality
all individuals: 1230
bin: 7.75e1
variant carriers: 977

GenotypeQuality
all individuals: 118
bin: 1.25e1
variant carriers: 81

GenotypeQuality
all individuals: 1169
bin: 6.25e1
variant carriers: 864

GenotypeQuality
all individuals: 200
bin: 1.75e1
variant carriers: 165

GenotypeQuality
all individuals: 212
bin: 2.5e0
variant carriers: 53

GenotypeQuality
all individuals: 1286
bin: 8.25e1
variant carriers: 1060

GenotypeQuality
all individuals: 953
bin: 5.25e1
variant carriers: 806

GenotypeQuality
all individuals: 797
bin: 8.75e1
variant carriers: 656

GenotypeQuality
all individuals: 318
bin: 2.75e1
variant carriers: 208

GenotypeQuality
all individuals: 620
bin: 7.25e1
variant carriers: 494

GenotypeQuality
all individuals: 1471
bin: 9.25e1
variant carriers: 1260

GenotypeQuality
all individuals: 378
bin: 2.25e1
variant carriers: 238

European (Non-Finnish)
type: Population
allele count: 51124
allele frequency: 7.800427220018309e-1
allele num: 65540
num of homozygotes: 19884

Other
type: Population
allele count: 659
allele frequency: 7.471655328798186e-1
allele num: 882
num of homozygotes: 249

Latino
type: Population
allele count: 9054
allele frequency: 7.958860759493671e-1
allele num: 11376
num of homozygotes: 3610

European (Finnish)
type: Population
allele count: 5254
allele frequency: 7.97752808988764e-1
allele num: 6586
num of homozygotes: 2086

East Asian
type: Population
allele count: 4770
allele frequency: 5.654338549075392e-1
allele num: 8436
num of homozygotes: 1350

African
type: Population
allele count: 6676
allele frequency: 6.898119446166563e-1
allele num: 9678
num of homozygotes: 2303

South Asian
type: Population
allele count: 10798
allele frequency: 6.810899457550145e-1
allele num: 15854
num of homozygotes: 3711

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.97e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e0

MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.79e-2

QD
type: SiteQuality
SIO_000300: 3.091e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

DP
type: SiteQuality
SIO_000300: 2.527892e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000387998
ensembl transcript: ENST00000429541
gene symbol: ZNF195
hgvsc: ENST00000429541.2:c.142+48C>G
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435828
ensembl transcript: ENST00000526601
gene symbol: ZNF195
hgvsc: ENST00000526601.1:c.142+48C>G
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 4468
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 704
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 415
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2679
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 239
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1428
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1550
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 481
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12063
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1009
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5943
bin: 2.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 6842
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 111
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9215
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 347
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1245
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11398
bin: 3.25e1
variant carriers: 4

GenotypeQuality
all individuals: 4614
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3081
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 107
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22914
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 5638
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10708
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4391
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3843
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2540
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9852
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
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: 10
allele frequency: 1.157407407407407e-3
allele num: 8640
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

QD
type: SiteQuality
SIO_000300: 1.239e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

VQSLOD
type: SiteQuality
SIO_000300: 4.47e0

DP
type: SiteQuality
SIO_000300: 2.313364e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.322e0

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000344483
ensembl transcript: ENST00000343338
gene symbol: ZNF195
hgvsc: ENST00000343338.7:c.142+45T>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000524857
gene symbol: ZNF195
hgvsc: ENST00000524857.1:n.295+45T>A
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 481
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 412
bin: 1.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 12067
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 240
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 704
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1172
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6162
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 346
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4468
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 6845
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1550
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11424
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2680
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1009
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1245
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9220
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4397
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4640
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3841
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22912
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 105
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5676
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 329
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11105
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2544
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3115
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.498500299940011e-5
allele num: 66680
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9854
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.944e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.99e-1

QD
type: SiteQuality
SIO_000300: 1.39e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.03e-1

DP
type: SiteQuality
SIO_000300: 2.314979e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -7.999000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

FS
type: SiteQuality
SIO_000300: 1.2091e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435153
ensembl transcript: ENST00000532539
gene symbol: ZNF195
hgvsc: ENST00000532539.1:c.142+35C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.316+35C>T
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 704
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1550
bin: 5.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 6856
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6440
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9255
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 481
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 346
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12157
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 350
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 604
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2683
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4468
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11639
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 167
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 240
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1245
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1009
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3117
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22920
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 101
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11820
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4423
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4619
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3853
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2555
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5694
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9854
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: 8640
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.619999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 3.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.168e0

VQSLOD
type: SiteQuality
SIO_000300: 5.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.847e0

DP
type: SiteQuality
SIO_000300: 2.321673e6

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000524857
gene symbol: ZNF195
hgvsc: ENST00000524857.1:n.295+21T>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000437265
ensembl transcript: ENST00000534569
gene symbol: ZNF195
hgvsc: ENST00000534569.1:c.142+21T>C
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 9304
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2685
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6535
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1010
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 240
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12312
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 704
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 139
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 481
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6878
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 1551
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11908
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 346
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1245
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4478
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5781
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4660
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22942
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12286
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 116
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 172
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3141
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2594
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4509
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66692
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
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: 16500
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: 9866
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.55e-1

FS
type: SiteQuality
SIO_000300: 6.117e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.93e0

MQ
type: SiteQuality
SIO_000300: 5.85e1

VQSLOD
type: SiteQuality
SIO_000300: -3.092e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-1

QD
type: SiteQuality
SIO_000300: 1.487e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: -3.97e-1

DP
type: SiteQuality
SIO_000300: 2.330995e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000431937
ensembl transcript: ENST00000528410
gene symbol: ZNF195
hgvsc: ENST00000528410.1:c.142+20G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435741
ensembl transcript: ENST00000525313
gene symbol: ZNF195
hgvsc: ENST00000525313.2:c.130+20G>A
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 4479
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 704
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 178
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6882
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11939
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9316
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 153
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 481
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 345
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 145
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6520
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 240
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1552
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 12316
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2685
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1246
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1010
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22942
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 137
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5763
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3903
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2593
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3127
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4496
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12280
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4652
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9866
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: 902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.314279102059708e-4
allele num: 8642
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.889e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

DP
type: SiteQuality
SIO_000300: 2.331918e6

MQRankSum
type: SiteQuality
SIO_000300: -6.13e-1

FS
type: SiteQuality
SIO_000300: 2.972e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 1.134e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 9.04e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000524857
gene symbol: ZNF195
hgvsc: ENST00000524857.1:n.295+19C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000436384
ensembl transcript: ENST00000528218
gene symbol: ZNF195
hgvsc: ENST00000528218.1:c.142+19C>T
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 132
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1552
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2687
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6493
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 481
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11958
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4480
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12334
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1010
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 150
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 161
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1245
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6885
bin: 4.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 345
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 704
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9326
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 240
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4508
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3137
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 56
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4655
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12314
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5770
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22948
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2596
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
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: 16502
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9866
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.731601731601732e-4
allele num: 11550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66690
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.332666e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.66e-1

QD
type: SiteQuality
SIO_000300: 1.221e1

FS
type: SiteQuality
SIO_000300: 4.205e0

VQSLOD
type: SiteQuality
SIO_000300: 4.23e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

MQ
type: SiteQuality
SIO_000300: 5.913e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000344483
ensembl transcript: ENST00000343338
gene symbol: ZNF195
hgvsc: ENST00000343338.7:c.142+16A>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.316+16A>T
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 2687
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12379
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9327
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1553
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 11972
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 154
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 481
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6484
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6885
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 140
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 128
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1010
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1245
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 346
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 704
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4480
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 240
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3151
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3912
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4673
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12361
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22955
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4526
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2601
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5814
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.012965964343598e-4
allele num: 9872
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 1.362e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e0

VQSLOD
type: SiteQuality
SIO_000300: 3.17e-1

QD
type: SiteQuality
SIO_000300: 1.295e1

DP
type: SiteQuality
SIO_000300: 2.33364e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000524857
gene symbol: ZNF195
hgvsc: ENST00000524857.1:n.295+16A>G
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: true
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000382511
ensembl transcript: ENST00000399602
gene symbol: ZNF195
hgvsc: ENST00000399602.4:c.130+16A>G
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 1245
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 128
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1010
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4480
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6484
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6885
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11972
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 240
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 704
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2687
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 154
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 118
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1553
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 346
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 9327
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 140
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12379
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 481
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3912
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5814
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4526
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2601
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4673
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22955
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3151
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12361
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.731002250302925e-4
allele num: 11554
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66702
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 6.32e-1

FS
type: SiteQuality
SIO_000300: 1.362e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 2.33364e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.295e1

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000436384
ensembl transcript: ENST00000528218
gene symbol: ZNF195
hgvsc: ENST00000528218.1:c.142+7A>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000431937
ensembl transcript: ENST00000528410
gene symbol: ZNF195
hgvsc: ENST00000528410.1:c.142+7A>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434715
ensembl transcript: ENST00000529678
gene symbol: ZNF195
hgvsc: ENST00000529678.1:c.142+7A>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: splice_region_variant
consequence: intron_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435741
ensembl transcript: ENST00000525313
gene symbol: ZNF195
hgvsc: ENST00000525313.2:c.130+7A>T
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 2686
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 89
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 241
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 72
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6890
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6479
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 345
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 704
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 481
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12418
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12027
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1245
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1012
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4482
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1551
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9346
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3166
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3916
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2606
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4689
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5832
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22958
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12449
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4537
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.817520901490367e-4
allele num: 16506
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9884
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
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.335963e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-2

QD
type: SiteQuality
SIO_000300: 8.470000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.935e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.71e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000529085
gene symbol: ZNF195
hgvsc: ENST00000529085.1:n.221G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434715
ensembl transcript: ENST00000529678
gene symbol: ZNF195
hgvsc: ENST00000529678.1:c.139G>A
hgvsp: ENSP00000434715.1:p.Val47Ile
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000436384
ensembl transcript: ENST00000528218
gene symbol: ZNF195
hgvsc: ENST00000528218.1:c.139G>A
hgvsp: ENSP00000436384.1:p.Val47Ile
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000527386
gene symbol: ZNF195
hgvsc: ENST00000527386.1:n.487G>A
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 1013
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6353
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 345
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1554
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 482
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6905
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12079
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12509
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 703
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9367
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 171
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4490
bin: 4.75e1
variant carriers: 2

GenotypeDepth
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1245
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 240
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2685
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4704
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2606
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12450
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3173
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22969
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 4544
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5836
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3920
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.493780162465154e-5
allele num: 66722
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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: 2.33851e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 1.836e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.493e0

MQRankSum
type: SiteQuality
SIO_000300: 4.65e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.95e-1

QD
type: SiteQuality
SIO_000300: 1.116e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.49e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000346613
ensembl transcript: ENST00000354599
gene symbol: ZNF195
hgvsc: ENST00000354599.6:c.126C>T
hgvsp: ENST00000354599.6:c.126C>T(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000387998
ensembl transcript: ENST00000429541
gene symbol: ZNF195
hgvsc: ENST00000429541.2:c.138C>T
hgvsp: ENST00000429541.2:c.138C>T(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000527386
gene symbol: ZNF195
hgvsc: ENST00000527386.1:n.486C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435153
ensembl transcript: ENST00000532539
gene symbol: ZNF195
hgvsc: ENST00000532539.1:c.138C>T
hgvsp: ENST00000532539.1:c.138C>T(p.%3D)
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 1763
bin: 5.75e1
variant carriers: 318

GenotypeDepth
all individuals: 86
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4565
bin: 4.75e1
variant carriers: 288

GenotypeDepth
all individuals: 48
bin: 1.75e1
variant carriers: 5

GenotypeDepth
all individuals: 57
bin: 1.25e1
variant carriers: 2

GenotypeDepth
all individuals: 170
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 12097
bin: 2.75e1
variant carriers: 34

GenotypeDepth
all individuals: 6100
bin: 2.25e1
variant carriers: 12

GenotypeDepth
all individuals: 477
bin: 7.75e1
variant carriers: 159

GenotypeDepth
all individuals: 9066
bin: 3.75e1
variant carriers: 128

GenotypeDepth
all individuals: 1207
bin: 6.25e1
variant carriers: 266

GenotypeDepth
all individuals: 2825
bin: 5.25e1
variant carriers: 305

GenotypeDepth
all individuals: 227
bin: 9.25e1
variant carriers: 76

GenotypeDepth
all individuals: 11648
bin: 3.25e1
variant carriers: 64

GenotypeDepth
all individuals: 609
bin: 7.25e1
variant carriers: 164

GenotypeDepth
all individuals: 247
bin: 8.75e1
variant carriers: 72

GenotypeDepth
all individuals: 6763
bin: 4.25e1
variant carriers: 199

GenotypeDepth
all individuals: 333
bin: 8.25e1
variant carriers: 116

GenotypeDepth
all individuals: 1516
bin: 9.75e1
variant carriers: 340

GenotypeDepth
all individuals: 895
bin: 6.75e1
variant carriers: 242

GenotypeQuality
all individuals: 3717
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 188
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4496
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4334
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 5641
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24279
bin: 9.75e1
variant carriers: 2779

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2472
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3035
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12192
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 176
allele frequency: 2.661022074387662e-2
allele num: 6614
num of homozygotes: 1

South Asian
type: Population
allele count: 29
allele frequency: 1.756936871440688e-3
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 101
allele frequency: 8.738536078906385e-3
allele num: 11558
num of homozygotes: 1

African
type: Population
allele count: 52
allele frequency: 5.248284214775939e-3
allele num: 9908
num of homozygotes: 0

Other
type: Population
allele count: 26
allele frequency: 2.876106194690265e-2
allele num: 904
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 2459
allele frequency: 3.686767219406879e-2
allele num: 66698
num of homozygotes: 51

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.34e-2

MQ
type: SiteQuality
SIO_000300: 5.965e1

DP
type: SiteQuality
SIO_000300: 2.411407e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.68e-1

QD
type: SiteQuality
SIO_000300: 1.413e1

FS
type: SiteQuality
SIO_000300: 5.649999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.52e0

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000524857
gene symbol: ZNF195
hgvsc: ENST00000524857.1:n.287T>G
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435741
ensembl transcript: ENST00000525313
gene symbol: ZNF195
hgvsc: ENST00000525313.2:c.122T>G
hgvsp: ENSP00000435741.1:p.Phe41Cys
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000437265
ensembl transcript: ENST00000534569
gene symbol: ZNF195
hgvsc: ENST00000534569.1:c.134T>G
hgvsp: ENSP00000437265.1:p.Phe45Cys
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000433911
ensembl transcript: ENST00000533036
gene symbol: ZNF195
hgvsc: ENST00000533036.1:c.122T>G
hgvsp: ENSP00000433911.1:p.Phe41Cys
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 776
bin: 6.75e1
variant carriers: 2

GenotypeDepth
all individuals: 9267
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1303
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 515
bin: 7.25e1
variant carriers: 3

GenotypeDepth
all individuals: 83
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 12381
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 51
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4632
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 11879
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 168
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 378
bin: 7.75e1
variant carriers: 3

GenotypeDepth
all individuals: 6121
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1082
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 171
bin: 9.25e1
variant carriers: 2

GenotypeDepth
all individuals: 6899
bin: 4.25e1
variant carriers: 2

GenotypeDepth
all individuals: 1686
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2806
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 80
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4637
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3879
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3143
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5853
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4486
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23175
bin: 9.75e1
variant carriers: 17

GenotypeQuality
all individuals: 12517
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2577
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

African
type: Population
allele count: 17
allele frequency: 1.713709677419355e-3
allele num: 9920
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.363525e6

VQSLOD
type: SiteQuality
SIO_000300: 2.7e0

QD
type: SiteQuality
SIO_000300: 1.454e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.39e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 1.794e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.93e-1

Annotation
canonical: true
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000382511
ensembl transcript: ENST00000399602
gene symbol: ZNF195
hgvsc: ENST00000399602.4:c.117C>T
hgvsp: ENST00000399602.4:c.117C>T(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.303C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000414353
ensembl transcript: ENST00000438262
gene symbol: ZNF195
hgvsc: ENST00000438262.2:c.129C>T
hgvsp: ENST00000438262.2:c.129C>T(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000437265
ensembl transcript: ENST00000534569
gene symbol: ZNF195
hgvsc: ENST00000534569.1:c.129C>T
hgvsp: ENST00000534569.1:c.129C>T(p.%3D)
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 190
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 176
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 71
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 375
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 775
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4635
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6897
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 12395
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2806
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 170
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 11895
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6095
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 56
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1082
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1687
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9270
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1301
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 515
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12500
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5845
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3880
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4483
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2577
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23169
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 195
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4638
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3149
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9930
num of homozygotes: 0

East Asian
type: Population
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: 2
allele frequency: 1.211240310077519e-4
allele num: 16512
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.07e1

DP
type: SiteQuality
SIO_000300: 2.36339e6

FS
type: SiteQuality
SIO_000300: 4.083e0

MQRankSum
type: SiteQuality
SIO_000300: -2.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.649e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.1e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434006
ensembl transcript: ENST00000525502
gene symbol: ZNF195
hgvsc: ENST00000525502.1:c.84G>T
hgvsp: ENSP00000434006.1:p.Leu28Phe
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.270G>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: true
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000382511
ensembl transcript: ENST00000399602
gene symbol: ZNF195
hgvsc: ENST00000399602.4:c.84G>T
hgvsp: ENSP00000382511.4:p.Leu28Phe
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000524857
gene symbol: ZNF195
hgvsc: ENST00000524857.1:n.249G>T
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 36
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1301
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6057
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9278
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 515
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 776
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1081
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 76
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12423
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1685
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 190
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 195
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4639
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11899
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 169
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6907
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 375
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2804
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23170
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 21
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3879
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12568
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4479
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3136
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5857
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2576
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4640
bin: 7.75e1
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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49902563333833e-5
allele num: 66710
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9984
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.0232e1

MQ
type: SiteQuality
SIO_000300: 5.834e1

DP
type: SiteQuality
SIO_000300: 2.364198e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.917e0

MQRankSum
type: SiteQuality
SIO_000300: 3.18e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.0e-2

QD
type: SiteQuality
SIO_000300: 7.98e0

VQSLOD
type: SiteQuality
SIO_000300: -1.567e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000433911
ensembl transcript: ENST00000533036
gene symbol: ZNF195
hgvsc: ENST00000533036.1:c.82T>C
hgvsp: ENST00000533036.1:c.82T>C(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000524857
gene symbol: ZNF195
hgvsc: ENST00000524857.1:n.247T>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435741
ensembl transcript: ENST00000525313
gene symbol: ZNF195
hgvsc: ENST00000525313.2:c.82T>C
hgvsp: ENST00000525313.2:c.82T>C(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.268T>C
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 6053
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 515
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 776
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 46
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 6906
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1081
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 190
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2804
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4639
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12421
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1685
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1301
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 375
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11895
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 169
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9272
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12550
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4480
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5850
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23169
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4638
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3139
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3879
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2576
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

East Asian
type: Population
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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9988
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 2.7243e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.54e0

QD
type: SiteQuality
SIO_000300: 1.325e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.911e0

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

DP
type: SiteQuality
SIO_000300: 2.363872e6

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434715
ensembl transcript: ENST00000529678
gene symbol: ZNF195
hgvsc: ENST00000529678.1:c.94T>A
hgvsp: ENSP00000434715.1:p.Leu32Met
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000005082
ensembl transcript: ENST00000005082
gene symbol: ZNF195
hgvsc: ENST00000005082.9:c.82T>A
hgvsp: ENSP00000005082.9:p.Leu28Met
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000524857
gene symbol: ZNF195
hgvsc: ENST00000524857.1:n.247T>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000390663
ensembl transcript: ENST00000427810
gene symbol: ZNF195
hgvsc: ENST00000427810.2:c.127T>A
hgvsp: ENSP00000390663.2:p.Leu43Met
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 11895
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 169
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4639
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 8.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 515
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6906
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 36
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 199
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1685
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2804
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1081
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9272
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12421
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 46
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 776
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6053
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1301
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 375
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 190
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4638
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23169
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4480
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3139
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2576
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3879
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5850
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12550
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66708
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9988
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: 904
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

FS
type: SiteQuality
SIO_000300: 2.7243e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.911e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

DP
type: SiteQuality
SIO_000300: 2.363872e6

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

QD
type: SiteQuality
SIO_000300: 1.325e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.54e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000527386
gene symbol: ZNF195
hgvsc: ENST00000527386.1:n.435G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000432720
ensembl transcript: ENST00000528796
gene symbol: ZNF195
hgvsc: ENST00000528796.1:c.75G>A
hgvsp: ENST00000528796.1:c.75G>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.261G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000529085
gene symbol: ZNF195
hgvsc: ENST00000529085.1:n.169G>A
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4639
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6906
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 190
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 515
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 169
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6050
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1686
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9270
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1301
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 207
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 375
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11883
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1082
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2803
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 97
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 775
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12404
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12517
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2574
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23167
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3135
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4477
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5840
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4631
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3878
bin: 9.25e1
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: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9988
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499295331194339e-5
allele num: 66698
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.024e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.671e0

DP
type: SiteQuality
SIO_000300: 2.363314e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.912e1

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

VQSLOD
type: SiteQuality
SIO_000300: 2.81e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

FS
type: SiteQuality
SIO_000300: 2.155e0

QD
type: SiteQuality
SIO_000300: 1.244e1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.246C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000529085
gene symbol: ZNF195
hgvsc: ENST00000529085.1:n.154C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000527386
gene symbol: ZNF195
hgvsc: ENST00000527386.1:n.420C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000433911
ensembl transcript: ENST00000533036
gene symbol: ZNF195
hgvsc: ENST00000533036.1:c.60C>T
hgvsp: ENST00000533036.1:c.60C>T(p.%3D)
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 38
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2803
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12284
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1303
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 238
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 11776
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 515
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6169
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 170
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 190
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 159
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9259
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 777
bin: 6.75e1
variant carriers: 2

GenotypeDepth
all individuals: 6898
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 375
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1685
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4639
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1081
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12536
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2569
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4606
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3877
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4467
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5754
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23169
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 47
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3101
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9984
num of homozygotes: 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: 16430
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66676
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: 5
allele frequency: 4.320027648176948e-4
allele num: 11574
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.37e0

DP
type: SiteQuality
SIO_000300: 2.360442e6

QD
type: SiteQuality
SIO_000300: 8.949999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.436e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.876e0

FS
type: SiteQuality
SIO_000300: 1.166e0

VQSLOD
type: SiteQuality
SIO_000300: -1.847e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000433911
ensembl transcript: ENST00000533036
gene symbol: ZNF195
hgvsc: ENST00000533036.1:c.45G>A
hgvsp: ENST00000533036.1:c.45G>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000524857
gene symbol: ZNF195
hgvsc: ENST00000524857.1:n.210G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434715
ensembl transcript: ENST00000529678
gene symbol: ZNF195
hgvsc: ENST00000529678.1:c.57G>A
hgvsp: ENST00000529678.1:c.57G>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.231G>A
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 1685
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12071
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11647
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 4639
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 516
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 191
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 9229
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 333
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 169
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6896
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1081
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 259
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2803
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 375
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6214
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 776
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1305
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3873
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 4444
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 71
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4556
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5634
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 559
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23170
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 12371
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3048
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2560
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: 8
allele frequency: 9.246417013407304e-4
allele num: 8652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9960
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16260
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.055e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.56e-1

DP
type: SiteQuality
SIO_000300: 2.354227e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 5.0e-2

FS
type: SiteQuality
SIO_000300: 5.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.678e0

VQSLOD
type: SiteQuality
SIO_000300: 8.3e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000005082
ensembl transcript: ENST00000005082
gene symbol: ZNF195
hgvsc: ENST00000005082.9:c.27G>A
hgvsp: ENST00000005082.9:c.27G>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000524857
gene symbol: ZNF195
hgvsc: ENST00000524857.1:n.192G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000346613
ensembl transcript: ENST00000354599
gene symbol: ZNF195
hgvsc: ENST00000354599.6:c.27G>A
hgvsp: ENST00000354599.6:c.27G>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000432720
ensembl transcript: ENST00000528796
gene symbol: ZNF195
hgvsc: ENST00000528796.1:c.27G>A
hgvsp: ENST00000528796.1:c.27G>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 5949
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 866
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4640
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 269
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6878
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11552
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 777
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 169
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1685
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1080
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 190
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9196
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11438
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 632
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2805
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 515
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 375
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1301
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5467
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3865
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11662
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23159
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 173
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4421
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4496
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 184
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1263
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2989
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2550
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.007861318282604e-4
allele num: 9922
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15752
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66414
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 9.09e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.925e1

QD
type: SiteQuality
SIO_000300: 1.15e1

DP
type: SiteQuality
SIO_000300: 2.336312e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.833e0

MQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.52e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.201G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000437265
ensembl transcript: ENST00000534569
gene symbol: ZNF195
hgvsc: ENST00000534569.1:c.27G>A
hgvsp: ENST00000534569.1:c.27G>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000529085
gene symbol: ZNF195
hgvsc: ENST00000529085.1:n.109G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: synonymous_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000005082
ensembl transcript: ENST00000005082
gene symbol: ZNF195
hgvsc: ENST00000005082.9:c.15G>A
hgvsp: ENST00000005082.9:c.15G>A(p.%3D)
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 6868
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 390
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 980
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2805
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9167
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1673
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1684
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11141
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 169
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 375
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10814
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 777
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 152
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 5696
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1081
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 4639
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 190
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 515
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1306
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 23160
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 10657
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3857
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2199
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5245
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4410
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4440
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2927
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2545
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.646031471554557e-5
allele num: 11566
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66200
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 8.097165991902834e-4
allele num: 9880
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
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15164
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.33e-1

FS
type: SiteQuality
SIO_000300: 2.61e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.53e-1

DP
type: SiteQuality
SIO_000300: 2.314533e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e-1

QD
type: SiteQuality
SIO_000300: 1.415e1

MQ
type: SiteQuality
SIO_000300: 5.942e1

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000432552
ensembl transcript: ENST00000526501
gene symbol: ZNF195
hgvsc: ENST00000526501.1:c.14C>T
hgvsp: ENSP00000432552.1:p.Thr5Met
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000346613
ensembl transcript: ENST00000354599
gene symbol: ZNF195
hgvsc: ENST00000354599.6:c.14C>T
hgvsp: ENSP00000346613.6:p.Thr5Met
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: missense_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435741
ensembl transcript: ENST00000525313
gene symbol: ZNF195
hgvsc: ENST00000525313.2:c.14C>T
hgvsp: ENSP00000435741.1:p.Thr5Met
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: non_coding_transcript_exon_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000524857
gene symbol: ZNF195
hgvsc: ENST00000524857.1:n.179C>T
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 1913
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 515
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 165
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6866
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 408
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5632
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11072
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1080
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10608
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 777
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1064
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9156
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 190
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4637
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1686
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2805
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 375
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1302
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 170
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5192
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2917
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3857
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10297
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2419
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2544
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4428
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4409
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23154
bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66154
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
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15044
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.013581998783702e-4
allele num: 9866
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.903e0

VQSLOD
type: SiteQuality
SIO_000300: 3.97e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e-1

MQ
type: SiteQuality
SIO_000300: 5.983e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 9.13e-1

QD
type: SiteQuality
SIO_000300: 1.393e1

DP
type: SiteQuality
SIO_000300: 2.308285e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000434715
ensembl transcript: ENST00000529678
gene symbol: ZNF195
hgvsc: ENST00000529678.1:c.16-13_16-11delGTT
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000433911
ensembl transcript: ENST00000533036
gene symbol: ZNF195
hgvsc: ENST00000533036.1:c.4-13_4-11delGTT
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 9352
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1459
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2807
bin: 5.25e1
variant carriers: 13

GenotypeDepth
all individuals: 380
bin: 7.75e1
variant carriers: 7

GenotypeDepth
all individuals: 259
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6858
bin: 4.25e1
variant carriers: 11

GenotypeDepth
all individuals: 1699
bin: 5.75e1
variant carriers: 14

GenotypeDepth
all individuals: 172
bin: 9.25e1
variant carriers: 2

GenotypeDepth
all individuals: 10744
bin: 3.25e1
variant carriers: 2

GenotypeDepth
all individuals: 4988
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 366
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9119
bin: 3.75e1
variant carriers: 10

GenotypeDepth
all individuals: 192
bin: 8.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1307
bin: 9.75e1
variant carriers: 6

GenotypeDepth
all individuals: 4638
bin: 4.75e1
variant carriers: 12

GenotypeDepth
all individuals: 786
bin: 6.75e1
variant carriers: 12

GenotypeDepth
all individuals: 780
bin: 1.75e1
variant carriers: 2

GenotypeDepth
all individuals: 3136
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1089
bin: 6.25e1
variant carriers: 11

GenotypeDepth
all individuals: 520
bin: 7.25e1
variant carriers: 6

GenotypeQuality
all individuals: 640
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23226
bin: 9.75e1
variant carriers: 113

GenotypeQuality
all individuals: 131
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4895
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8546
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3347
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4387
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2868
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4395
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2537
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3852
bin: 9.25e1
variant carriers: 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: 0
allele frequency: 0.0e0
allele num: 65864
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.152073732718894e-3
allele num: 868
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.035002035002035e-4
allele num: 9828
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.125850340136054e-4
allele num: 14112
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

East Asian
type: Population
allele count: 107
allele frequency: 1.240435891490842e-2
allele num: 8626
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.63e0

VQSLOD
type: SiteQuality
SIO_000300: 3.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQ
type: SiteQuality
SIO_000300: 5.814e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.87e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.13e-1

DP
type: SiteQuality
SIO_000300: 2.275961e6

QD
type: SiteQuality
SIO_000300: 1.615e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-1

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000527386
gene symbol: ZNF195
hgvsc: ENST00000527386.1:n.364-23T>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435741
ensembl transcript: ENST00000525313
gene symbol: ZNF195
hgvsc: ENST00000525313.2:c.4-23T>A
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 1062
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1829
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 513
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6858
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 519
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2989
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1697
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9082
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9047
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4786
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 773
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 261
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4644
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1302
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2805
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 170
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 376
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1088
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10642
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8086
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2851
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4389
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3852
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23169
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 663
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 667
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2544
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4383
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3265
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4768
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13436
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.525087692542321e-5
allele num: 65570
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.331e1

VQSLOD
type: SiteQuality
SIO_000300: -1.415e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.919999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.661e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 2.262459e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.82e-1

MQ
type: SiteQuality
SIO_000300: 5.914e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435153
ensembl transcript: ENST00000532539
gene symbol: ZNF195
hgvsc: ENST00000532539.1:c.16-25G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000431937
ensembl transcript: ENST00000528410
gene symbol: ZNF195
hgvsc: ENST00000528410.1:c.16-25G>A
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 1902
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10628
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2910
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1088
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9076
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4753
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4648
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1178
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 376
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 170
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 773
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 545
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1697
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2803
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6866
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 261
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8946
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1302
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 513
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3087
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4381
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 754
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7849
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2844
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4742
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23168
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4381
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 460
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3850
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2542
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9772
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: 1.526857422053929e-5
allele num: 65494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13136
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.573e0

DP
type: SiteQuality
SIO_000300: 2.260264e6

MQ
type: SiteQuality
SIO_000300: 5.949e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 3.08e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.088e0

MQRankSum
type: SiteQuality
SIO_000300: 1.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.449e0

QD
type: SiteQuality
SIO_000300: 1.958e1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435153
ensembl transcript: ENST00000532539
gene symbol: ZNF195
hgvsc: ENST00000532539.1:c.16-33A>G
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: non_coding_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl transcript: ENST00000330692
gene symbol: ZNF195
hgvsc: ENST00000330692.7:n.190-33A>G
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 2804
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2492
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 10439
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5139
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6861
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4648
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 773
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1088
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 513
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 578
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9053
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8529
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1297
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1302
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2382
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 376
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 261
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1697
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 170
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 193
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4367
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3846
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2088
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 826
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4470
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 921
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6292
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 884
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23168
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4383
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2541
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2802
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.607587160190447e-5
allele num: 65110
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-2

FS
type: SiteQuality
SIO_000300: 3.648e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.604e0

VQSLOD
type: SiteQuality
SIO_000300: 8.129999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.68e-1

QD
type: SiteQuality
SIO_000300: 1.147e1

MQ
type: SiteQuality
SIO_000300: 5.947e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.35e-1

DP
type: SiteQuality
SIO_000300: 2.250723e6

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000005082
ensembl transcript: ENST00000005082
gene symbol: ZNF195
hgvsc: ENST00000005082.9:c.4-38G>A
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000387998
ensembl transcript: ENST00000429541
gene symbol: ZNF195
hgvsc: ENST00000429541.2:c.16-38G>A
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 1696
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 377
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2348
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8628
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 576
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4647
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2538
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4982
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1088
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 775
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9057
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 261
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 512
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 10462
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6875
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1286
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2808
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 170
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1302
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1794
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 919
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5712
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 668
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4377
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2544
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3844
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23165
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 384
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 592
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2773
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1167
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4292
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4332
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65002
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11804
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.691117677733357e-5
allele num: 11506
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.257e0

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.1e-3

QD
type: SiteQuality
SIO_000300: 1.945e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.84e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 2.251358e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000414353
ensembl transcript: ENST00000438262
gene symbol: ZNF195
hgvsc: ENST00000438262.2:c.16-39C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: NMD_transcript_variant
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000432552
ensembl transcript: ENST00000526501
gene symbol: ZNF195
hgvsc: ENST00000526501.1:c.4-39C>T
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 1972
bin: 6.75e1
variant carriers: 1945

GenotypeDepth
all individuals: 495
bin: 8.75e1
variant carriers: 487

GenotypeDepth
all individuals: 516
bin: 2.5e0
variant carriers: 281

GenotypeDepth
all individuals: 2094
bin: 2.25e1
variant carriers: 1769

GenotypeDepth
all individuals: 6754
bin: 4.75e1
variant carriers: 6453

GenotypeDepth
all individuals: 2648
bin: 7.5e0
variant carriers: 2161

GenotypeDepth
all individuals: 1316
bin: 1.75e1
variant carriers: 1177

GenotypeDepth
all individuals: 2945
bin: 6.25e1
variant carriers: 2879

GenotypeDepth
all individuals: 648
bin: 8.25e1
variant carriers: 629

GenotypeDepth
all individuals: 408
bin: 9.25e1
variant carriers: 391

GenotypeDepth
all individuals: 2338
bin: 1.25e1
variant carriers: 2120

GenotypeDepth
all individuals: 3837
bin: 2.75e1
variant carriers: 3152

GenotypeDepth
all individuals: 1353
bin: 7.25e1
variant carriers: 1327

GenotypeDepth
all individuals: 7066
bin: 3.75e1
variant carriers: 6427

GenotypeDepth
all individuals: 5731
bin: 3.25e1
variant carriers: 4951

GenotypeDepth
all individuals: 4207
bin: 5.75e1
variant carriers: 4109

GenotypeDepth
all individuals: 2146
bin: 9.75e1
variant carriers: 2077

GenotypeDepth
all individuals: 5546
bin: 5.25e1
variant carriers: 5369

GenotypeDepth
all individuals: 7529
bin: 4.25e1
variant carriers: 7061

GenotypeDepth
all individuals: 958
bin: 7.75e1
variant carriers: 939

GenotypeQuality
all individuals: 341
bin: 5.75e1
variant carriers: 290

GenotypeQuality
all individuals: 1274
bin: 8.25e1
variant carriers: 967

GenotypeQuality
all individuals: 935
bin: 2.25e1
variant carriers: 701

GenotypeQuality
all individuals: 583
bin: 1.75e1
variant carriers: 507

GenotypeQuality
all individuals: 416
bin: 2.5e0
variant carriers: 23

GenotypeQuality
all individuals: 292
bin: 4.25e1
variant carriers: 244

GenotypeQuality
all individuals: 576
bin: 3.75e1
variant carriers: 490

GenotypeQuality
all individuals: 437
bin: 5.25e1
variant carriers: 392

GenotypeQuality
all individuals: 325
bin: 7.5e0
variant carriers: 146

GenotypeQuality
all individuals: 446
bin: 2.75e1
variant carriers: 369

GenotypeQuality
all individuals: 691
bin: 3.25e1
variant carriers: 620

GenotypeQuality
all individuals: 426
bin: 4.75e1
variant carriers: 367

GenotypeQuality
all individuals: 47706
bin: 9.75e1
variant carriers: 46492

GenotypeQuality
all individuals: 253
bin: 1.25e1
variant carriers: 180

GenotypeQuality
all individuals: 1029
bin: 6.25e1
variant carriers: 455

GenotypeQuality
all individuals: 1389
bin: 9.25e1
variant carriers: 1134

GenotypeQuality
all individuals: 1101
bin: 7.75e1
variant carriers: 771

GenotypeQuality
all individuals: 589
bin: 7.25e1
variant carriers: 379

GenotypeQuality
all individuals: 881
bin: 6.75e1
variant carriers: 507

GenotypeQuality
all individuals: 817
bin: 8.75e1
variant carriers: 670

Latino
type: Population
allele count: 9138
allele frequency: 7.96131730266597e-1
allele num: 11478
num of homozygotes: 3665

African
type: Population
allele count: 6235
allele frequency: 6.434468524251806e-1
allele num: 9690
num of homozygotes: 2009

European (Non-Finnish)
type: Population
allele count: 50614
allele frequency: 7.793483616654349e-1
allele num: 64944
num of homozygotes: 19700

European (Finnish)
type: Population
allele count: 5273
allele frequency: 7.989393939393939e-1
allele num: 6600
num of homozygotes: 2096

East Asian
type: Population
allele count: 4868
allele frequency: 5.697565543071161e-1
allele num: 8544
num of homozygotes: 1399

Other
type: Population
allele count: 629
allele frequency: 7.505966587112172e-1
allele num: 838
num of homozygotes: 239

South Asian
type: Population
allele count: 8365
allele frequency: 6.90523361400033e-1
allele num: 12114
num of homozygotes: 2866

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

FS
type: SiteQuality
SIO_000300: 9.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.78e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e-1

DP
type: SiteQuality
SIO_000300: 2.734984e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.033e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.758e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.09e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.52e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000344483
ensembl transcript: ENST00000343338
gene symbol: ZNF195
hgvsc: ENST00000343338.7:c.16-49C>T
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435828
ensembl transcript: ENST00000526601
gene symbol: ZNF195
hgvsc: ENST00000526601.1:c.16-49C>T
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 2053
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1479
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2230
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 3556
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8853
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3229
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 4006
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 482
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 211
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8643
bin: 3.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 1971
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1181
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 249
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6833
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 944
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1356
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 608
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5251
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7078
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5641
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1149
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4230
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 815
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1667
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1040
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1399
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 360
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1167
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4244
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21135
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1887
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1568
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4261
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3752
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2422
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2204
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10530
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.10539718029936e-5
allele num: 64404
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.323e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.299708e6

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.821e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.13e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.57e-1

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000433911
ensembl transcript: ENST00000533036
gene symbol: ZNF195
hgvsc: ENST00000533036.1:c.4-52G>C
variant of: http://identifiers.org/hgnc/12986

Annotation
canonical: false
consequence: intron_variant
ensembl gene: ENSG00000005801
ensembl protein: ENSP00000435153
ensembl transcript: ENST00000532539
gene symbol: ZNF195
hgvsc: ENST00000532539.1:c.16-52G>C
variant of: http://identifiers.org/hgnc/12986

GenotypeDepth
all individuals: 2049
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3558
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3255
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2230
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 249
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 5245
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1959
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8553
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1184
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 6958
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 8581
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7074
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4239
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 482
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 211
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 943
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1356
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 608
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1478
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1058
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1196
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1341
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 841
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2203
bin: 5.25e1
variant carriers: 0