1-249144644-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144644
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144644
    reference: chr 1
allele count: 12
allele frequency: 9.959828690946516e-5
allele num: 120484
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.759C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*213C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*624C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1340C>T
  hgvsp: ENSP00000391200.1:p.Thr447Met
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.585C>T
  hgvsp: ENSP00000431582.1:p.Thr196Met
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1190C>T
  hgvsp: ENSP00000355427.3:p.Thr397Met
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1322C>T
  hgvsp: ENSP00000355425.5:p.Thr441Met
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1190C>T
  hgvsp: ENSP00000390044.1:p.Thr397Met
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1590C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1325C>T
  hgvsp: ENSP00000305483.4:p.Thr442Met
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.806C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*1035C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1570C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1381C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7352
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1249
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Thr447Met
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

1-249144645-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144645
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144645
    reference: chr 1
allele count: 3
allele frequency: 2.48970920196521e-5
allele num: 120496
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1321A>G
  hgvsp: ENSP00000355425.5:p.Thr441Ala
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.584A>G
  hgvsp: ENSP00000431582.1:p.Thr196Ala
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*1034A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*623A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1324A>G
  hgvsp: ENSP00000305483.4:p.Thr442Ala
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1339A>G
  hgvsp: ENSP00000391200.1:p.Thr447Ala
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*212A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1189A>G
  hgvsp: ENSP00000355427.3:p.Thr397Ala
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1569A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1189A>G
  hgvsp: ENSP00000390044.1:p.Thr397Ala
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1380A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1589A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.758A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.805A>G
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Thr447Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP

1-249144653-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144653
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144653
    reference: chr 1
allele count: 1
allele frequency: 8.323345318950592e-6
allele num: 120144
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.576A>G
  hgvsp: ENSP00000431582.1:p.His193Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*204A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1561A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.750A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1316A>G
  hgvsp: ENSP00000305483.4:p.His439Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*615A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.797A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*1026A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1331A>G
  hgvsp: ENSP00000391200.1:p.His444Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1181A>G
  hgvsp: ENSP00000355427.3:p.His394Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1313A>G
  hgvsp: ENSP00000355425.5:p.His438Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1372A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1181A>G
  hgvsp: ENSP00000390044.1:p.His394Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1581A>G
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28657
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 613
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His444Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

1-249144658-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144658
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144658
    reference: chr 1
allele count: 1
allele frequency: 8.33694600993764e-6
allele num: 119948
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1176C>T
  hgvsp: ENST00000366471.3:c.1176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1308C>T
  hgvsp: ENST00000366469.5:c.1308C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*1021C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1176C>T
  hgvsp: ENST00000427146.1:c.1176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.745C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1556C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1311C>T
  hgvsp: ENST00000306601.4:c.1311C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*199C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1367C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.571C>T
  hgvsp: ENST00000476503.1:c.571C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1326C>T
  hgvsp: ENST00000451251.1:c.1326C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*610C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1576C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.792C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg442Arg
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

1-249144659-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144659
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144659
    reference: chr 1
allele count: 1
allele frequency: 8.342649291709075e-6
allele num: 119866
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1555G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.791G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1310G>A
  hgvsp: ENSP00000305483.4:p.Arg437His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1325G>A
  hgvsp: ENSP00000391200.1:p.Arg442His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1175G>A
  hgvsp: ENSP00000390044.1:p.Arg392His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.570G>A
  hgvsp: ENSP00000431582.1:p.Arg191His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1175G>A
  hgvsp: ENSP00000355427.3:p.Arg392His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*609G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1575G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*198G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*1020G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.744G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1307G>A
  hgvsp: ENSP00000355425.5:p.Arg436His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1366G>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg442His
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

1-249144660-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144660
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144660
    reference: chr 1
allele count: 1
allele frequency: 8.347663488989432e-6
allele num: 119794
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1174C>T
  hgvsp: ENSP00000390044.1:p.Arg392Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1324C>T
  hgvsp: ENSP00000391200.1:p.Arg442Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1574C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1365C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1554C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*197C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1174C>T
  hgvsp: ENSP00000355427.3:p.Arg392Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1306C>T
  hgvsp: ENSP00000355425.5:p.Arg436Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.569C>T
  hgvsp: ENSP00000431582.1:p.Arg191Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1309C>T
  hgvsp: ENSP00000305483.4:p.Arg437Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.790C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*608C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*1019C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.743C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 764
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg442Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum

1-249144661-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144661
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144661
    reference: chr 1
allele count: 1
allele frequency: 8.348499774590506e-6
allele num: 119782
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.789G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1308G>A
  hgvsp: ENST00000306601.4:c.1308G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1323G>A
  hgvsp: ENST00000451251.1:c.1323G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1305G>A
  hgvsp: ENST00000366469.5:c.1305G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1364G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1173G>A
  hgvsp: ENST00000427146.1:c.1173G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*607G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1553G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1573G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.568G>A
  hgvsp: ENST00000476503.1:c.568G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*1018G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.742G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*196G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1173G>A
  hgvsp: ENST00000366471.3:c.1173G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln441Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

1-249144663-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144663
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144663
    reference: chr 1
allele count: 1
allele frequency: 8.357709987463435e-6
allele num: 119650
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1321C>A
  hgvsp: ENSP00000391200.1:p.Gln441Lys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.566C>A
  hgvsp: ENSP00000431582.1:p.Gln190Lys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1551C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1306C>A
  hgvsp: ENSP00000305483.4:p.Gln436Lys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1571C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1362C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*1016C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1171C>A
  hgvsp: ENSP00000355427.3:p.Gln391Lys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1171C>A
  hgvsp: ENSP00000390044.1:p.Gln391Lys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*194C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.787C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1303C>A
  hgvsp: ENSP00000355425.5:p.Gln435Lys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*605C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.740C>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7162
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln441Lys
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/1-249144681-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144681
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144681
    reference: chr 1
allele count: 2
allele frequency: 1.697591118203269e-5
allele num: 117814
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1303G>T
  hgvsp: ENSP00000391200.1:p.Ala435Ser
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1344G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*587G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*176G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.548G>T
  hgvsp: ENSP00000431582.1:p.Ala184Ser
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1153G>T
  hgvsp: ENSP00000355427.3:p.Ala385Ser
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.722G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.769G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1553G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1153G>T
  hgvsp: ENSP00000390044.1:p.Ala385Ser
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1533G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*998G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1288G>T
  hgvsp: ENSP00000305483.4:p.Ala430Ser
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1285G>T
  hgvsp: ENSP00000355425.5:p.Ala429Ser
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3084
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala435Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

1-249144689-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144689
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144689
    reference: chr 1
allele count: 3
allele frequency: 2.573296049132799e-5
allele num: 116582
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.714G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1145G>A
  hgvsp: ENSP00000390044.1:p.Arg382His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1295G>A
  hgvsp: ENSP00000391200.1:p.Arg432His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*168G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.761G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.540G>A
  hgvsp: ENSP00000431582.1:p.Arg181His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1280G>A
  hgvsp: ENSP00000305483.4:p.Arg427His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1525G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*990G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1277G>A
  hgvsp: ENSP00000355425.5:p.Arg426His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1145G>A
  hgvsp: ENSP00000355427.3:p.Arg382His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1545G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1336G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*579G>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1752
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16689
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg432His
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

1-249144690-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144690
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144690
    reference: chr 1
allele count: 1
allele frequency: 8.582954252853832e-6
allele num: 116510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.760C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.539C>T
  hgvsp: ENSP00000431582.1:p.Arg181Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1294C>T
  hgvsp: ENSP00000391200.1:p.Arg432Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.713C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*989C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1144C>T
  hgvsp: ENSP00000355427.3:p.Arg382Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1335C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1276C>T
  hgvsp: ENSP00000355425.5:p.Arg426Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*578C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1144C>T
  hgvsp: ENSP00000390044.1:p.Arg382Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*167C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1544C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1279C>T
  hgvsp: ENSP00000305483.4:p.Arg427Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1524C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6357
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg432Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-249144696-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144696
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144696
    reference: chr 1
allele count: 12
allele frequency: 1.043877657538537e-4
allele num: 114956
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1273A>C
  hgvsp: ENSP00000305483.4:p.Thr425Pro
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*161A>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1518A>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1288A>C
  hgvsp: ENSP00000391200.1:p.Thr430Pro
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1138A>C
  hgvsp: ENSP00000390044.1:p.Thr380Pro
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1270A>C
  hgvsp: ENSP00000355425.5:p.Thr424Pro
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1538A>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.533A>C
  hgvsp: ENSP00000431582.1:p.Thr179Pro
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.754A>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1138A>C
  hgvsp: ENSP00000355427.3:p.Thr380Pro
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*572A>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*983A>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.707A>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1329A>C
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15759
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24450
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr430Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum

1-249144703-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144703
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144703
    reference: chr 1
allele count: 5
allele frequency: 4.398543202491335e-5
allele num: 113674
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1263C>T
  hgvsp: ENST00000366469.5:c.1263C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.700C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1266C>T
  hgvsp: ENST00000306601.4:c.1266C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1131C>T
  hgvsp: ENST00000427146.1:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.747C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1511C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1131C>T
  hgvsp: ENST00000366471.3:c.1131C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1531C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1322C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1281C>T
  hgvsp: ENST00000451251.1:c.1281C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.526C>T
  hgvsp: ENST00000476503.1:c.526C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*976C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*565C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*154C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7551
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys427Cys
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: G
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD

1-249144707-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144707
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144707
    reference: chr 1
allele count: 1
allele frequency: 8.843609607697478e-6
allele num: 113076
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*561T>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*150T>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.696T>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.522T>C
  hgvsp: ENSP00000431582.1:p.Ile175Thr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.743T>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1277T>C
  hgvsp: ENSP00000391200.1:p.Ile426Thr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1507T>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1127T>C
  hgvsp: ENSP00000390044.1:p.Ile376Thr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1318T>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1127T>C
  hgvsp: ENSP00000355427.3:p.Ile376Thr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1527T>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1262T>C
  hgvsp: ENSP00000305483.4:p.Ile421Thr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1259T>C
  hgvsp: ENSP00000355425.5:p.Ile420Thr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*972T>C
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22004
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8624
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15161
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile426Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

1-249144719-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144719
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144719
    reference: chr 1
allele count: 6
allele frequency: 5.455636581861827e-5
allele num: 109978
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1519-4C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-4C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1269-4C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1499-4C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.688-4C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1254-4C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*553-4C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1119-4C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.735-4C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1251-4C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*142-4C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*964-4C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.514-4C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1119-4C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17046
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5644
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1269-4C>T
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD

1-249144723-CAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144723
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144721
    reference: chr 1
allele count: 1
allele frequency: 9.159857839006339e-6
allele num: 109172
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.688-10_688-9delCT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-10_1310-9delCT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1119-10_1119-9delCT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1519-10_1519-9delCT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1251-10_1251-9delCT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.514-10_514-9delCT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1269-10_1269-9delCT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.735-10_735-9delCT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*142-10_*142-9delCT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1254-10_1254-9delCT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*553-10_*553-9delCT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1119-10_1119-9delCT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1499-10_*1499-9delCT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*964-10_*964-9delCT
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6655
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: CAG
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

1-249144727-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144727
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144727
    reference: chr 1
allele count: 1
allele frequency: 9.245391172500508e-6
allele num: 108162
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-12C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1254-12C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*964-12C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*553-12C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1499-12C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1519-12C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.688-12C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1269-12C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1251-12C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*142-12C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1119-12C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.514-12C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1119-12C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.735-12C>G
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8080
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5820
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

1-249144727-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144727
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144727
    reference: chr 1
allele count: 1
allele frequency: 9.245391172500508e-6
allele num: 108162
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1251-12C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1519-12C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*964-12C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.514-12C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*553-12C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-12C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1254-12C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1119-12C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.688-12C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1499-12C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1269-12C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*142-12C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.735-12C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1119-12C>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5820
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8080
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12979
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16186
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

1-249144729-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144729
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144729
    reference: chr 1
allele count: 39
allele frequency: 3.618952174155114e-4
allele num: 107766
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*553-14G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*142-14G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1119-14G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1519-14G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-14G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.735-14G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.514-14G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1499-14G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1251-14G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1269-14G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*964-14G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1119-14G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.688-14G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1254-14G>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5900
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11574
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16471
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2834
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12549
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

1-249144731-GAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144731
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144729
    reference: chr 1
allele count: 1
allele frequency: 9.308906761989872e-6
allele num: 107424
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.688-18_688-17delTT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1269-18_1269-17delTT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.514-18_514-17delTT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.735-18_735-17delTT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1499-18_*1499-17delTT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*142-18_*142-17delTT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*964-18_*964-17delTT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1254-18_1254-17delTT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-18_1310-17delTT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1519-18_1519-17delTT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*553-18_*553-17delTT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1119-18_1119-17delTT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1119-18_1119-17delTT
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1251-18_1251-17delTT
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11425
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17006
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6087
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: GAA
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS

1-249144736-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144736
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144736
    reference: chr 1
allele count: 29
allele frequency: 2.723516153268219e-4
allele num: 106480
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1519-21C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*964-21C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1269-21C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1499-21C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1251-21C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.688-21C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*142-21C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1254-21C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1119-21C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.514-21C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.735-21C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*553-21C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1119-21C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-21C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10429
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10746
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17639
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6350
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/1-249144745-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144745
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144745
    reference: chr 1
allele count: 1
allele frequency: 9.574875526618154e-6
allele num: 104440
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1519-30G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.514-30G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.735-30G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.688-30G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*553-30G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1269-30G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1499-30G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*142-30G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-30G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1254-30G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*964-30G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1251-30G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1119-30G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1119-30G>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7003
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13312
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17996
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9560
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ

1-249144750-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144750
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144750
    reference: chr 1
allele count: 7
allele frequency: 6.755061471059387e-5
allele num: 103626
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1254-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*142-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1499-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*964-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1119-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.688-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1519-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*553-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1269-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.735-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1119-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1251-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.514-35G>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14297
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6340
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum

1-249144753-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144753
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144753
    reference: chr 1
allele count: 1
allele frequency: 9.728951413616641e-6
allele num: 102786
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1519-38G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.688-38G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1269-38G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1119-38G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*553-38G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-38G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*964-38G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1254-38G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.514-38G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1499-38G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1119-38G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1251-38G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.735-38G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*142-38G>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9427
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14735
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17738
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

1-249144834-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144834
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144834
    reference: chr 1
allele count: 7
allele frequency: 5.824984189328629e-5
allele num: 120172
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*141+47G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1118+47G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.734+47G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-119G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.513+47G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1518+47G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*963+47G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1253+47G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1268+47G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.687+47G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1498+47G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*552+47G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1118+47G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1250+47G>C
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2832
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20219
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15635
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6457
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9049
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

1-249144839-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144839
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144839
    reference: chr 1
allele count: 9
allele frequency: 7.480674923115286e-5
allele num: 120310
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.513+42G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*141+42G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1268+42G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1498+42G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.687+42G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1518+42G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1250+42G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1253+42G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.734+42G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1118+42G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*552+42G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1118+42G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-124G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*963+42G>C
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9217
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17111
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20685
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum

1-249144859-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144859
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144859
    reference: chr 1
allele count: 1
allele frequency: 8.27787159365584e-6
allele num: 120804
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.513+22G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*963+22G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1118+22G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-144G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1498+22G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.734+22G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*141+22G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1268+22G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1253+22G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1518+22G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.687+22G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1250+22G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*552+22G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1118+22G>C
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22700
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

1-249144864-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144864
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144864
    reference: chr 1
allele count: 4
allele frequency: 3.309066843150232e-5
allele num: 120880
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1518+17G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1253+17G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*552+17G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.734+17G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1250+17G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1118+17G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1268+17G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1118+17G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*963+17G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.513+17G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*141+17G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-149G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.687+17G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1498+17G>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

1-249144866-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144866
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144866
    reference: chr 1
allele count: 1
allele frequency: 8.268699664290793e-6
allele num: 120938
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*552+15G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-151G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1518+15G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.734+15G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1498+15G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*141+15G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1118+15G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1118+15G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*963+15G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1250+15G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.687+15G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1253+15G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1268+15G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.513+15G>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23130
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

1-249144875-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144875
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144875
    reference: chr 1
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*141+6T>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1250+6T>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1118+6T>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1518+6T>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*552+6T>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1253+6T>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-160T>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.687+6T>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.513+6T>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1268+6T>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.734+6T>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1118+6T>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1498+6T>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*963+6T>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1268+6T>A
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: QD

1-249144881-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144881
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144881
    reference: chr 1
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1518A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1498A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1118A>G
  hgvsp: ENSP00000355427.3:p.Gln373Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1253A>G
  hgvsp: ENSP00000305483.4:p.Gln418Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.687A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1268A>G
  hgvsp: ENSP00000391200.1:p.Gln423Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*552A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1118A>G
  hgvsp: ENSP00000390044.1:p.Gln373Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*141A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1250A>G
  hgvsp: ENSP00000355425.5:p.Gln417Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.734A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-166A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.513A>G
  hgvsp: ENSP00000431582.1:p.Gln172Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*963A>G
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23717
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln423Arg
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum

1-249144893-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144893
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144893
    reference: chr 1
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-178A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1238A>G
  hgvsp: ENSP00000355425.5:p.Glu413Gly
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.722A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*951A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1486A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1106A>G
  hgvsp: ENSP00000390044.1:p.Glu369Gly
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1106A>G
  hgvsp: ENSP00000355427.3:p.Glu369Gly
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1241A>G
  hgvsp: ENSP00000305483.4:p.Glu414Gly
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1506A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1256A>G
  hgvsp: ENSP00000391200.1:p.Glu419Gly
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.501A>G
  hgvsp: ENSP00000431582.1:p.Glu168Gly
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*129A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.675A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*540A>G
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9854
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu419Gly
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

1-249144897-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144897
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144897
    reference: chr 1
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.718G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1237G>A
  hgvsp: ENSP00000305483.4:p.Gly413Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1102G>A
  hgvsp: ENSP00000390044.1:p.Gly368Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*125G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1252G>A
  hgvsp: ENSP00000391200.1:p.Gly418Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*536G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.671G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*947G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1234G>A
  hgvsp: ENSP00000355425.5:p.Gly412Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1102G>A
  hgvsp: ENSP00000355427.3:p.Gly368Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-182G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1502G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.497G>A
  hgvsp: ENSP00000431582.1:p.Gly167Arg
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1482G>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly418Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

1-249144903-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144903
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144903
    reference: chr 1
allele count: 2
allele frequency: 1.648804616652927e-5
allele num: 121300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*941C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1228C>T
  hgvsp: ENSP00000355425.5:p.His410Tyr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.665C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1096C>T
  hgvsp: ENSP00000355427.3:p.His366Tyr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*119C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-188C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1096C>T
  hgvsp: ENSP00000390044.1:p.His366Tyr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1246C>T
  hgvsp: ENSP00000391200.1:p.His416Tyr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1476C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*530C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.491C>T
  hgvsp: ENSP00000431582.1:p.His165Tyr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1231C>T
  hgvsp: ENSP00000305483.4:p.His411Tyr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1496C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.712C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His416Tyr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

1-249144908-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144908
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144908
    reference: chr 1
allele count: 2
allele frequency: 1.648723063986942e-5
allele num: 121306
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.486G>C
  hgvsp: ENSP00000431582.1:p.Arg163Pro
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*525G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1491G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1471G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.707G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*114G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1091G>C
  hgvsp: ENSP00000355427.3:p.Arg364Pro
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*936G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.660G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1091G>C
  hgvsp: ENSP00000390044.1:p.Arg364Pro
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1226G>C
  hgvsp: ENSP00000305483.4:p.Arg409Pro
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1223G>C
  hgvsp: ENSP00000355425.5:p.Arg408Pro
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-193G>C
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1241G>C
  hgvsp: ENSP00000391200.1:p.Arg414Pro
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23907
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg414Pro
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

1-249144908-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144908
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144908
    reference: chr 1
allele count: 4
allele frequency: 3.297446127973885e-5
allele num: 121306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*936G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1226G>A
  hgvsp: ENSP00000305483.4:p.Arg409His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1223G>A
  hgvsp: ENSP00000355425.5:p.Arg408His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1091G>A
  hgvsp: ENSP00000390044.1:p.Arg364His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.660G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*114G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*525G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1241G>A
  hgvsp: ENSP00000391200.1:p.Arg414His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1491G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1471G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1091G>A
  hgvsp: ENSP00000355427.3:p.Arg364His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.486G>A
  hgvsp: ENSP00000431582.1:p.Arg163His
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-193G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.707G>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23907
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg414His
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS

1-249144909-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144909
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144909
    reference: chr 1
allele count: 3
allele frequency: 2.473166147301776e-5
allele num: 121302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.659C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*524C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1240C>T
  hgvsp: ENSP00000391200.1:p.Arg414Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1222C>T
  hgvsp: ENSP00000355425.5:p.Arg408Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.485C>T
  hgvsp: ENSP00000431582.1:p.Arg163Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*935C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1090C>T
  hgvsp: ENSP00000355427.3:p.Arg364Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1090C>T
  hgvsp: ENSP00000390044.1:p.Arg364Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1225C>T
  hgvsp: ENSP00000305483.4:p.Arg409Cys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1470C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1490C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*113C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-194C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.706C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg414Cys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

1-249144914-TGGATGACAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144914
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144905
    reference: chr 1
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.645_653delTTGTCATCC
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsp: ENSP00000355427.3:p.Leu359_Ile361del
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.692_700delTTGTCATCC
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.471_479delTTGTCATCC
  hgvsp: ENSP00000431582.1:p.Leu158_Ile160del
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsp: ENSP00000355425.5:p.Leu403_Ile405del
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsp: ENSP00000305483.4:p.Leu404_Ile406del
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsp: ENSP00000390044.1:p.Leu359_Ile361del
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsp: ENSP00000391200.1:p.Leu409_Ile411del
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu409_Ile411del
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
reference allele: TGGATGACAA
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

1-249144925-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144925
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144925
    reference: chr 1
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1206C>T
  hgvsp: ENST00000366469.5:c.1206C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1474C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1454C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1209C>T
  hgvsp: ENST00000306601.4:c.1209C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-210C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*97C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1224C>T
  hgvsp: ENST00000451251.1:c.1224C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*919C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.469C>T
  hgvsp: ENST00000476503.1:c.469C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1074C>T
  hgvsp: ENST00000427146.1:c.1074C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1074C>T
  hgvsp: ENST00000366471.3:c.1074C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*508C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.643C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.690C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20635
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn408Asn
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

1-249144925-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144925
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144925
    reference: chr 1
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*97C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.643C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1209C>A
  hgvsp: ENSP00000305483.4:p.Asn403Lys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1454C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.469C>A
  hgvsp: ENSP00000431582.1:p.Asn157Lys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*919C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1474C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*508C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1224C>A
  hgvsp: ENSP00000391200.1:p.Asn408Lys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-210C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1206C>A
  hgvsp: ENSP00000355425.5:p.Asn402Lys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1074C>A
  hgvsp: ENSP00000390044.1:p.Asn358Lys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1074C>A
  hgvsp: ENSP00000355427.3:p.Asn358Lys
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.690C>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20635
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9859
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn408Lys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

1-249144931-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144931
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144931
    reference: chr 1
allele count: 3
allele frequency: 2.473533194815474e-5
allele num: 121284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*91C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.463C>T
  hgvsp: ENST00000476503.1:c.463C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1203C>T
  hgvsp: ENST00000306601.4:c.1203C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1200C>T
  hgvsp: ENST00000366469.5:c.1200C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1068C>T
  hgvsp: ENST00000427146.1:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1068C>T
  hgvsp: ENST00000366471.3:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1448C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1218C>T
  hgvsp: ENST00000451251.1:c.1218C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1468C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-216C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*502C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.684C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*913C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.637C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20599
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser406Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

1-249144933-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144933
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144933
    reference: chr 1
allele count: 260
allele frequency: 2.143976251339985e-3
allele num: 121270
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1198A>G
  hgvsp: ENSP00000355425.5:p.Ser400Gly
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*500A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.682A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1201A>G
  hgvsp: ENSP00000305483.4:p.Ser401Gly
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1066A>G
  hgvsp: ENSP00000390044.1:p.Ser356Gly
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1466A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1446A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*911A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1216A>G
  hgvsp: ENSP00000391200.1:p.Ser406Gly
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-218A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*89A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1066A>G
  hgvsp: ENSP00000355427.3:p.Ser356Gly
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.635A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.461A>G
  hgvsp: ENSP00000431582.1:p.Ser155Gly
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 20515
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 5.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
hgvs: p.Ser406Gly
num of homozygotes: 4
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

1-249144935-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144935
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144935
    reference: chr 1
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.459C>T
  hgvsp: ENSP00000431582.1:p.Thr154Ile
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1064C>T
  hgvsp: ENSP00000355427.3:p.Thr355Ile
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*498C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1064C>T
  hgvsp: ENSP00000390044.1:p.Thr355Ile
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-220C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.633C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1444C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1214C>T
  hgvsp: ENSP00000391200.1:p.Thr405Ile
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*87C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1199C>T
  hgvsp: ENSP00000305483.4:p.Thr400Ile
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*909C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1464C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.680C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1196C>T
  hgvsp: ENSP00000355425.5:p.Thr399Ile
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr405Ile
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

1-249144937-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144937
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144937
    reference: chr 1
allele count: 2
allele frequency: 1.649348507339601e-5
allele num: 121260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1062C>T
  hgvsp: ENST00000427146.1:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1197C>T
  hgvsp: ENST00000306601.4:c.1197C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*496C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1062C>T
  hgvsp: ENST00000366471.3:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*85C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1194C>T
  hgvsp: ENST00000366469.5:c.1194C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1212C>T
  hgvsp: ENST00000451251.1:c.1212C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*907C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-222C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.457C>T
  hgvsp: ENST00000476503.1:c.457C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.678C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1462C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.631C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1442C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg404Arg
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

1-249144937-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144937
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144937
    reference: chr 1
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1062C>A
  hgvsp: ENST00000366471.3:c.1062C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1194C>A
  hgvsp: ENST00000366469.5:c.1194C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.678C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1062C>A
  hgvsp: ENST00000427146.1:c.1062C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*907C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*85C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1442C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.457C>A
  hgvsp: ENST00000476503.1:c.457C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.631C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1212C>A
  hgvsp: ENST00000451251.1:c.1212C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-222C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1197C>A
  hgvsp: ENST00000306601.4:c.1197C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*496C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1462C>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9881
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24046
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg404Arg
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD

1-249144947-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144947
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144947
    reference: chr 1
allele count: 5
allele frequency: 4.127592127856294e-5
allele num: 121136
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*897G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*486G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.668G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1184G>A
  hgvsp: ENSP00000355425.5:p.Arg395Gln
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1052G>A
  hgvsp: ENSP00000355427.3:p.Arg351Gln
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1202G>A
  hgvsp: ENSP00000391200.1:p.Arg401Gln
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1452G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1187G>A
  hgvsp: ENSP00000305483.4:p.Arg396Gln
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*75G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.447G>A
  hgvsp: ENSP00000431582.1:p.Arg150Gln
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-232G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1052G>A
  hgvsp: ENSP00000390044.1:p.Arg351Gln
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1432G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.621G>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg401Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

1-249144948-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144948
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144948
    reference: chr 1
allele count: 4
allele frequency: 3.302728053372085e-5
allele num: 121112
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-233C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1186C>T
  hgvsp: ENSP00000305483.4:p.Arg396Trp
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1201C>T
  hgvsp: ENSP00000391200.1:p.Arg401Trp
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1051C>T
  hgvsp: ENSP00000355427.3:p.Arg351Trp
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.667C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*485C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.620C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*74C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1051C>T
  hgvsp: ENSP00000390044.1:p.Arg351Trp
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1183C>T
  hgvsp: ENSP00000355425.5:p.Arg395Trp
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*896C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.446C>T
  hgvsp: ENSP00000431582.1:p.Arg150Trp
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1451C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1431C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24038
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9894
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2607
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg401Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum

1-249144951-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144951
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144951
    reference: chr 1
allele count: 2
allele frequency: 1.652018766933192e-5
allele num: 121064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*893G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1183G>A
  hgvsp: ENSP00000305483.4:p.Ala395Thr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1048G>A
  hgvsp: ENSP00000355427.3:p.Ala350Thr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1180G>A
  hgvsp: ENSP00000355425.5:p.Ala394Thr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1048G>A
  hgvsp: ENSP00000390044.1:p.Ala350Thr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.443G>A
  hgvsp: ENSP00000431582.1:p.Ala149Thr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.664G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1448G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1198G>A
  hgvsp: ENSP00000391200.1:p.Ala400Thr
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-236G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.617G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*71G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*482G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1428G>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9867
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala400Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

1-249144952-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144952
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144952
    reference: chr 1
allele count: 3
allele frequency: 2.47843759294141e-5
allele num: 121044
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.616C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1179C>T
  hgvsp: ENST00000366469.5:c.1179C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-237C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1447C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1197C>T
  hgvsp: ENST00000451251.1:c.1197C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1427C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*481C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1182C>T
  hgvsp: ENST00000306601.4:c.1182C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*892C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*70C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1047C>T
  hgvsp: ENST00000427146.1:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.663C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1047C>T
  hgvsp: ENST00000366471.3:c.1047C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.442C>T
  hgvsp: ENST00000476503.1:c.442C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys399Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

1-249144955-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144955
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144955
    reference: chr 1
allele count: 1
allele frequency: 8.266785708380868e-6
allele num: 120966
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*478C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*889C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1044C>A
  hgvsp: ENSP00000390044.1:p.Phe348Leu
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1179C>A
  hgvsp: ENSP00000305483.4:p.Phe393Leu
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-240C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1044C>A
  hgvsp: ENSP00000355427.3:p.Phe348Leu
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1194C>A
  hgvsp: ENSP00000391200.1:p.Phe398Leu
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.613C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1176C>A
  hgvsp: ENSP00000355425.5:p.Phe392Leu
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*67C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1444C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.439C>A
  hgvsp: ENSP00000431582.1:p.Phe147Leu
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.660C>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1424C>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe398Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/1-249144962-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144962
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144962
    reference: chr 1
allele count: 19
allele frequency: 1.57482925535442e-4
allele num: 120648
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1037G>T
  hgvsp: ENSP00000355427.3:p.Cys346Phe
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1417G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1169G>T
  hgvsp: ENSP00000355425.5:p.Cys390Phe
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1172G>T
  hgvsp: ENSP00000305483.4:p.Cys391Phe
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.653G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1187G>T
  hgvsp: ENSP00000391200.1:p.Cys396Phe
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.606G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*471G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1037G>T
  hgvsp: ENSP00000390044.1:p.Cys346Phe
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1437G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-247G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.432G>T
  hgvsp: ENSP00000431582.1:p.Cys145Phe
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*60G>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*882G>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19831
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Cys396Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

1-249144970-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144970
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144970
    reference: chr 1
allele count: 2
allele frequency: 1.666277868497351e-5
allele num: 120028
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1161C>G
  hgvsp: ENSP00000355425.5:p.Asp387Glu
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1409C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.424C>G
  hgvsp: ENSP00000431582.1:p.Asp142Glu
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1429C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1179C>G
  hgvsp: ENSP00000391200.1:p.Asp393Glu
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.645C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.598C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1029C>G
  hgvsp: ENSP00000390044.1:p.Asp343Glu
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*52C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-255C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1029C>G
  hgvsp: ENSP00000355427.3:p.Asp343Glu
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*874C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*463C>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1164C>G
  hgvsp: ENSP00000305483.4:p.Asp388Glu
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp393Glu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

1-249144974-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144974
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144974
    reference: chr 1
allele count: 1
allele frequency: 8.360644772924887e-6
allele num: 119608
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1025G>A
  hgvsp: ENSP00000390044.1:p.Arg342Gln
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1405G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*870G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1175G>A
  hgvsp: ENSP00000391200.1:p.Arg392Gln
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*48G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*459G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1157G>A
  hgvsp: ENSP00000355425.5:p.Arg386Gln
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1025G>A
  hgvsp: ENSP00000355427.3:p.Arg342Gln
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1425G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1160G>A
  hgvsp: ENSP00000305483.4:p.Arg387Gln
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.641G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.594G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.420G>A
  hgvsp: ENSP00000431582.1:p.Arg141Gln
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-259G>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 23449
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9821
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg392Gln
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP

1-249144975-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144975
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144975
    reference: chr 1
allele count: 4
allele frequency: 3.345880384776244e-5
allele num: 119550
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1404C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1024C>T
  hgvsp: ENSP00000355427.3:p.Arg342Trp
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1174C>T
  hgvsp: ENSP00000391200.1:p.Arg392Trp
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*869C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*47C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1424C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.593C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1159C>T
  hgvsp: ENSP00000305483.4:p.Arg387Trp
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1024C>T
  hgvsp: ENSP00000390044.1:p.Arg342Trp
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1156C>T
  hgvsp: ENSP00000355425.5:p.Arg386Trp
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-260C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.640C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.419C>T
  hgvsp: ENSP00000431582.1:p.Arg141Trp
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*458C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg392Trp
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

1-249144976-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144976
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144976
    reference: chr 1
allele count: 1
allele frequency: 8.391092016715055e-6
allele num: 119174
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*457C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1155C>T
  hgvsp: ENST00000366469.5:c.1155C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.418C>T
  hgvsp: ENST00000476503.1:c.418C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.639C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1173C>T
  hgvsp: ENST00000451251.1:c.1173C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1403C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-261C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*46C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1158C>T
  hgvsp: ENST00000306601.4:c.1158C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1423C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1023C>T
  hgvsp: ENST00000366471.3:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1023C>T
  hgvsp: ENST00000427146.1:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.592C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*868C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1091
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr391Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

1-249144977-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144977
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144977
    reference: chr 1
allele count: 1
allele frequency: 8.391092016715055e-6
allele num: 119174
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1022C>T
  hgvsp: ENSP00000390044.1:p.Thr341Ile
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.638C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1157C>T
  hgvsp: ENSP00000305483.4:p.Thr386Ile
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.591C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-262C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1022C>T
  hgvsp: ENSP00000355427.3:p.Thr341Ile
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1154C>T
  hgvsp: ENSP00000355425.5:p.Thr385Ile
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1402C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1172C>T
  hgvsp: ENSP00000391200.1:p.Thr391Ile
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*45C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1422C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.417C>T
  hgvsp: ENSP00000431582.1:p.Thr140Ile
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*456C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*867C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23307
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1092
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17980
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr391Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD

1-249144978-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144978
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144977
    reference: chr 1
allele count: 1
allele frequency: 8.391232839928842e-6
allele num: 119172
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*865delC
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1170delC
  hgvsp: ENSP00000391200.1:p.Asp390GlufsTer48
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1020delC
  hgvsp: ENSP00000390044.1:p.Asp340GlufsTer48
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*43delC
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1020delC
  hgvsp: ENSP00000355427.3:p.Asp340GlufsTer48
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1420delC
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1400delC
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1152delC
  hgvsp: ENSP00000355425.5:p.Asp384GlufsTer48
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.415delC
  hgvsp: ENSP00000431582.1:p.Asp139GlufsTer48
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.589delC
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1155delC
  hgvsp: ENSP00000305483.4:p.Asp385GlufsTer48
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.636delC
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-264delC
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*454delC
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9710
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1095
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp390GlufsTer48
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: TG
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

1-249144993-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144993
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144993
    reference: chr 1
allele count: 1
allele frequency: 8.745080891998251e-6
allele num: 114350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*864-13C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1399-13C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.635-13C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1151-13C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.414-13C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1419-13C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1019-13C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.588-13C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*42-13C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1019-13C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*453-13C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-278C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1169-13C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1154-13C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8854
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11933
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3359
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

1-249144997-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144997
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144997
    reference: chr 1
allele count: 1
allele frequency: 8.898855607168918e-6
allele num: 112374
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1151-17C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1399-17C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1169-17C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*42-17C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*864-17C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.414-17C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.635-17C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.588-17C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-282C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*453-17C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1419-17C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1154-17C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1019-17C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1019-17C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8187
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8994
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13981
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-249144999-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249144999
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249144999
    reference: chr 1
allele count: 1
allele frequency: 8.960091751339533e-6
allele num: 111606
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.588-19G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1399-19G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*42-19G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1019-19G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1151-19G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1419-19G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-284G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1169-19G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*453-19G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.414-19G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1019-19G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.635-19G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1154-19G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*864-19G>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

1-249145006-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249145006
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249145006
    reference: chr 1
allele count: 2
allele frequency: 1.853155924539491e-5
allele num: 107924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*42-26C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.414-26C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1019-26C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.588-26C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-291C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1419-26C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1169-26C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1399-26C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.635-26C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*453-26C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1019-26C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*864-26C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1151-26C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1154-26C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2190
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24014
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9215
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

1-249145015-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249145015
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249145015
    reference: chr 1
allele count: 1
allele frequency: 9.996001599360256e-6
allele num: 100040
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1019-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1169-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1399-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1154-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*42-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1419-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*453-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.588-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.414-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.635-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1019-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1151-35G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-300G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*864-35G>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7676
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9835
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum

1-249145022-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249145022
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249145022
    reference: chr 1
allele count: 1
allele frequency: 1.135383078250602e-5
allele num: 88076
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1169-42A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*863+40A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1399-42A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1019-42A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1151-42A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*41+40A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1019-42A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-307A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1154-42A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.635-42A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*453-42A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1419-42A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.414-42A>G
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.588-42A>G
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2833
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10617
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

1-249145026-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249145026
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249145026
    reference: chr 1
allele count: 4
allele frequency: 5.686503084927924e-5
allele num: 70342
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1154-46C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1019-46C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1151-46C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*863+36C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*453-46C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.635-46C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1169-46C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1019-46C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-311C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1419-46C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*41+36C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.414-46C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.588-46C>T
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1399-46C>T
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1717
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19287
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18238
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8811
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1847
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

1-249145030-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 249145030
    reference: chr 1
  end: Position
    type: ExactPosition
    position: 249145030
    reference: chr 1
allele count: 1
allele frequency: 1.67521023888498e-5
allele num: 59694
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355427
  ensembl transcript: ENST00000366471
  gene symbol: ZNF692
  hgvsc: ENST00000366471.3:c.1019-50G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000433522
  ensembl transcript: ENST00000482023
  gene symbol: ZNF692
  hgvsc: ENST00000482023.1:c.*41+32G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000533927
  gene symbol: ZNF692
  hgvsc: ENST00000533927.1:n.1419-50G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000393552
  ensembl transcript: ENST00000412341
  gene symbol: ZNF692
  hgvsc: ENST00000412341.2:c.*863+32G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000391200
  ensembl transcript: ENST00000451251
  gene symbol: ZNF692
  hgvsc: ENST00000451251.1:c.1169-50G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000390044
  ensembl transcript: ENST00000427146
  gene symbol: ZNF692
  hgvsc: ENST00000427146.1:c.1019-50G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000462037
  gene symbol: ZNF692
  hgvsc: ENST00000462037.2:n.588-50G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436814
  ensembl transcript: ENST00000477070
  gene symbol: ZNF692
  hgvsc: ENST00000477070.2:c.*453-50G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000470787
  gene symbol: ZNF692
  hgvsc: ENST00000470787.2:n.1310-315G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000436308
  ensembl transcript: ENST00000463519
  gene symbol: ZNF692
  hgvsc: ENST00000463519.1:c.*1399-50G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl transcript: ENST00000474351
  gene symbol: ZNF692
  hgvsc: ENST00000474351.1:n.635-50G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000431582
  ensembl transcript: ENST00000476503
  gene symbol: ZNF692
  hgvsc: ENST00000476503.1:c.414-50G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000355425
  ensembl transcript: ENST00000366469
  gene symbol: ZNF692
  hgvsc: ENST00000366469.5:c.1151-50G>A
  variant of: http://identifiers.org/hgnc/26049
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000171163
  ensembl protein: ENSP00000305483
  ensembl transcript: ENST00000306601
  gene symbol: ZNF692
  hgvsc: ENST00000306601.4:c.1154-50G>A
  variant of: http://identifiers.org/hgnc/26049
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 18643
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19709
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7753
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS

GenotypeDepth
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 538
bin: 4.25e1
variant carriers: 3

GenotypeDepth
all individuals: 701
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19811
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 76
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 40
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 84
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 843
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 194
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2017
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43061
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1010
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1788
bin: 9.75e1
variant carriers: 12

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

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

GenotypeQuality
all individuals: 7873
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.31535077564251e-4
allele num: 8638
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6460
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.535340748108629e-5
allele num: 66354
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.927525057825752e-4
allele num: 10376
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.849796522382538e-4
allele num: 16218
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.722e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.238e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.352e1

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
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VQSLOD
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MQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.514096235956757e-5
allele num: 66046
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

MQRankSum
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DP
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FS
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SIO_000300: 8.59e-1

ClippingRankSum
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BaseQRankSum
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MQ
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QD
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.063068582105553e-5
allele num: 65294
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.555305e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.66e-1

InbreedingCoeff
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FS
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BaseQRankSum
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MQ
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MQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 2
allele frequency: 2.35626767200754e-4
allele num: 8488
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.543019380323417e-5
allele num: 64808
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.522541e6

MQRankSum
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SIO_000300: 3.62e-1

ClippingRankSum
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MQ
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SIO_000300: 6.0e1

VQSLOD
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QD
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -8.0e-4

BaseQRankSum
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SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64764
num of homozygotes: 0

European (Finnish)
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allele count: 0
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num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.790483649892304e-5
allele num: 10214
num of homozygotes: 0

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

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

South Asian
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allele count: 0
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num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -5.545e-1

MQRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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FS
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SIO_000300: 7.143e0

QD
type: SiteQuality
SIO_000300: 8.699999999999999e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
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SIO_000300: 1.91e0

BaseQRankSum
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SIO_000300: 2.23e0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 1.490066225165563e-3
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 64084
num of homozygotes: 0

South Asian
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Other
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East Asian
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Latino
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allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: 3.66e0

InbreedingCoeff
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FS
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QD
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ClippingRankSum
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MQ
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ReadPosRankSum
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DP
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VQSLOD
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MQRankSum
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GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
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allele num: 63510
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East Asian
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South Asian
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allele num: 14164
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European (Finnish)
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Other
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Latino
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allele num: 10926
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MQ
type: SiteQuality
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QD
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FS
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DP
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.582228410493339e-5
allele num: 63202
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5934
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8180
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10040
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14066
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
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BaseQRankSum
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SIO_000300: 3.15e0

FS
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SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: -5.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.405508e6

GenotypeDepth
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variant carriers: 2

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 7.600709399543957e-4
allele num: 7894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5752
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13440
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61778
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.93e-1

InbreedingCoeff
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MQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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FS
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SIO_000300: 5.39e-1

DP
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SIO_000300: 1.28598e6

QD
type: SiteQuality
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5692
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10438
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13248
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7820
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.026904908605463e-4
allele num: 9738
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61452
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.512e0

QD
type: SiteQuality
SIO_000300: 1.577e1

BaseQRankSum
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SIO_000300: -1.799e0

DP
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SIO_000300: 1.249789e6

InbreedingCoeff
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SIO_000300: -2.0e-3

VQSLOD
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SIO_000300: 1.62e0

ClippingRankSum
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SIO_000300: -5.669999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.08e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

GenotypeDepth
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5650
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 7.634753397465261e-5
allele num: 13098
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60932
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.41e-1

QD
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BaseQRankSum
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MQ
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 5.355e0

ClippingRankSum
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SIO_000300: 5.29e-1

VQSLOD
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SIO_000300: 7.82e-1

DP
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SIO_000300: 1.202529e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13098
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 780
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60932
num of homozygotes: 0

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

Latino
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allele frequency: 9.704968944099378e-5
allele num: 10304
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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DP
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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FS
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QD
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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allele frequency: 0.0e0
allele num: 776
num of homozygotes: 0

European (Finnish)
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allele num: 5624
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South Asian
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African
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allele frequency: 1.036054703688355e-4
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European (Non-Finnish)
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allele frequency: 6.089933504509843e-4
allele num: 60756
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East Asian
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Latino
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DP
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FS
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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QD
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InbreedingCoeff
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MQ
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MQRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.651855033202286e-5
allele num: 60538
num of homozygotes: 0

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

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

MQRankSum
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QD
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DP
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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VQSLOD
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 1

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 5586
num of homozygotes: 0

South Asian
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allele count: 29
allele frequency: 2.259622876733676e-3
allele num: 12834
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60060
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59018
num of homozygotes: 0

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

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

African
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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VQSLOD
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MQRankSum
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FS
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QD
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MQ
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GenotypeDepth
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variant carriers: 5

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

Latino
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allele count: 3
allele frequency: 3.067484662576687e-4
allele num: 9780
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.833868653044489e-5
allele num: 58532
num of homozygotes: 0

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

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

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

DP
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ClippingRankSum
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InbreedingCoeff
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QD
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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FS
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MQ
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MQRankSum
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SIO_000300: 2.04e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele num: 5422
num of homozygotes: 0

European (Non-Finnish)
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South Asian
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num of homozygotes: 0

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

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

South Asian
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allele frequency: 2.430428970713331e-4
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East Asian
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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Other
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Latino
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BaseQRankSum
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MQRankSum
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FS
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DP
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MQ
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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Other
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Latino
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East Asian
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African
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European (Non-Finnish)
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BaseQRankSum
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ReadPosRankSum
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QD
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FS
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MQ
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MQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

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

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

East Asian
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num of homozygotes: 0

Other
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African
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allele frequency: 0.0e0
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South Asian
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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allele num: 66698
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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African
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Latino
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East Asian
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QD
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BaseQRankSum
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ReadPosRankSum
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MQ
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FS
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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Other
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MQRankSum
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QD
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VQSLOD
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InbreedingCoeff
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MQ
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DP
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BaseQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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European (Non-Finnish)
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South Asian
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East Asian
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European (Finnish)
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ClippingRankSum
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InbreedingCoeff
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QD
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DP
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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MQ
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FS
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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Latino
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East Asian
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African
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DP
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MQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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VQSLOD
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FS
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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East Asian
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South Asian
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African
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MQRankSum
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MQ
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VQSLOD
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FS
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ClippingRankSum
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QD
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ReadPosRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

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

ReadPosRankSum
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SIO_000300: 1.45e-1

FS
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MQ
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SIO_000300: 5.934e1

ClippingRankSum
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QD
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VQSLOD
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MQRankSum
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BaseQRankSum
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DP
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SIO_000300: 1.697389e6

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

European (Non-Finnish)
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allele num: 66698
num of homozygotes: 0

East Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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South Asian
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Other
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African
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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QD
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VQSLOD
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BaseQRankSum
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MQ
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.49829064955317e-5
allele num: 66692
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

East Asian
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South Asian
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Other
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DP
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InbreedingCoeff
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QD
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BaseQRankSum
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ReadPosRankSum
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FS
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SIO_000300: 9.202e0

VQSLOD
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MQ
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SIO_000300: 5.963e1

ClippingRankSum
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SIO_000300: -7.4e-2

MQRankSum
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SIO_000300: -4.74e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 256

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

East Asian
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allele count: 246
allele frequency: 2.847222222222222e-2
allele num: 8640
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African
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allele count: 0
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South Asian
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allele count: 9
allele frequency: 5.453884377651194e-4
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.49842555105713e-5
allele num: 66690
num of homozygotes: 0

Other
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allele num: 908
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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FS
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SIO_000300: 0.0e0

MQ
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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DP
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QD
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VQSLOD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele count: 0
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num of homozygotes: 0

African
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Other
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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ReadPosRankSum
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MQ
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FS
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MQRankSum
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BaseQRankSum
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QD
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DP
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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East Asian
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Latino
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ReadPosRankSum
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QD
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BaseQRankSum
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MQ
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FS
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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VQSLOD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Other
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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BaseQRankSum
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InbreedingCoeff
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DP
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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QD
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FS
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MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: 7.33e-1

GenotypeDepth
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variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11556
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: 6538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.818622696411251e-4
allele num: 16496
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.326e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
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SIO_000300: 2.76e0

ClippingRankSum
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SIO_000300: 6.21e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

DP
type: SiteQuality
SIO_000300: 1.695379e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501321162623108e-5
allele num: 66608
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.314279102059708e-4
allele num: 8642
num of homozygotes: 0

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

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

South Asian
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allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.695223e6

QD
type: SiteQuality
SIO_000300: 1.195e1

FS
type: SiteQuality
SIO_000300: 6.323e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.11e-1

VQSLOD
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SIO_000300: 7.53e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.69e-1

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.731601731601732e-4
allele num: 11550
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: 10374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66594
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -9.05e-1

VQSLOD
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SIO_000300: 2.09e-1

DP
type: SiteQuality
SIO_000300: 1.693795e6

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.934e1

FS
type: SiteQuality
SIO_000300: 6.748e0

BaseQRankSum
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SIO_000300: 6.69e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.12e0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.892960462873674e-4
allele num: 10370
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: 8640
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66586
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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QD
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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DP
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SIO_000300: 1.693451e6

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.93e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.47e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502448991856726e-5
allele num: 66558
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 898
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European (Finnish)
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East Asian
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allele frequency: 0.0e0
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South Asian
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African
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ReadPosRankSum
type: SiteQuality
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QD
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VQSLOD
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DP
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MQ
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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GenotypeDepth
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variant carriers: 2

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66422
num of homozygotes: 0

Latino
type: Population
allele count: 19
allele frequency: 1.65016501650165e-3
allele num: 11514
num of homozygotes: 0

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

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

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

East Asian
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allele count: 0
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ReadPosRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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MQ
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FS
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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MQRankSum
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QD
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GenotypeDepth
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variant carriers: 0

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

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

African
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allele count: 2
allele frequency: 1.956947162426615e-4
allele num: 10220
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6424
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.24e-1

MQ
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VQSLOD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 9.823182711198428e-5
allele num: 10180
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65880
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Other
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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VQSLOD
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FS
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BaseQRankSum
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MQ
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ClippingRankSum
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 65852
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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Other
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African
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allele num: 10174
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South Asian
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MQRankSum
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VQSLOD
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BaseQRankSum
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DP
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InbreedingCoeff
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FS
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ClippingRankSum
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ReadPosRankSum
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 65676
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East Asian
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African
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South Asian
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Other
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European (Finnish)
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Latino
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ReadPosRankSum
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MQ
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BaseQRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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DP
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 65678
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Other
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African
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European (Finnish)
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Latino
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South Asian
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East Asian
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DP
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FS
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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African
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MQ
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ReadPosRankSum
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QD
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InbreedingCoeff
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FS
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DP
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Latino
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Other
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European (Non-Finnish)
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African
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European (Finnish)
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DP
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MQ
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VQSLOD
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MQRankSum
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QD
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FS
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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East Asian
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South Asian
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African
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European (Finnish)
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MQ
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DP
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QD
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MQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Other
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East Asian
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South Asian
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European (Non-Finnish)
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DP
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FS
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QD
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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MQ
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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East Asian
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South Asian
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African
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VQSLOD
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QD
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DP
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MQRankSum
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ClippingRankSum
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MQ
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FS
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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Latino
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South Asian
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European (Finnish)
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European (Non-Finnish)
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East Asian
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DP
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VQSLOD
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MQ
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ClippingRankSum
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InbreedingCoeff
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FS
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QD
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BaseQRankSum
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South Asian
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European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.63e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.027e0

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.0719e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.01e-1

QD
type: SiteQuality
SIO_000300: 1.057e1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 2600
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 110
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1042
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 59
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 712
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 62
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1242
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6628
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1806
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12078
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1974
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3429
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 375
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14067
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7566
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2672
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 28
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3664
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4256
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.053062221408072e-5
allele num: 32754
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5088
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4396
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1914
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.855e1

QD
type: SiteQuality
SIO_000300: 2.51e0

MQRankSum
type: SiteQuality
SIO_000300: -1.02e0

VQSLOD
type: SiteQuality
SIO_000300: -2.984e0

FS
type: SiteQuality
SIO_000300: 0.0e0