16-89804338-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804338
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804338
    reference: chr 16
allele count: 1
allele frequency: 8.562376915831835e-6
allele num: 116790
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*21C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2250+25C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*474+25C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1562+25C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*671G>C
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1333+25C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1349+25C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.932+25C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*474+25C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.194+25C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1574+25C>G
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12674
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1758
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/16-89804339-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804339
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804339
    reference: chr 16
allele count: 663
allele frequency: 5.468853108090273e-3
allele num: 121232
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1574+26C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.194+26C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1333+26C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.932+26C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*474+26C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1562+26C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*670G>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*22C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2250+26C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*474+26C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1349+26C>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32582
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 3.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 11195
  bin: 3.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13150
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.25e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 52
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 22
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-89804339-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804339
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804338
    reference: chr 16
allele count: 1
allele frequency: 8.248647221855616e-6
allele num: 121232
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*474+27delA
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2250+27delA
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.932+27delA
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.194+27delA
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1349+27delA
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*474+27delA
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*669delT
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*23delA
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1574+27delA
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1562+27delA
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1333+27delA
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13150
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
reference allele: CA
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-89804343-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804343
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804343
    reference: chr 16
allele count: 2
allele frequency: 1.649402916144356e-5
allele num: 121256
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1574+30G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*474+30G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.194+30G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1333+30G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.932+30G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*666C>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*26G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1349+30G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*474+30G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1562+30G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2250+30G>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11320
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/16-89804344-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804344
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804344
    reference: chr 16
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1562+31C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1574+31C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2250+31C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*27C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1333+31C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.194+31C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*474+31C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*665G>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1349+31C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.932+31C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*474+31C>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13310
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

16-89804352-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804352
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804352
    reference: chr 16
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1563-32C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.195-32C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*475-32C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1575-32C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1350-32C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2251-32C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*35C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*657G>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.933-32C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*475-32C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1334-32C>T
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

16-89804353-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804353
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804353
    reference: chr 16
allele count: 1
allele frequency: 8.245790523937529e-6
allele num: 121274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1334-31T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*656A>C
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.933-31T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*475-31T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1563-31T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1575-31T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.195-31T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*36T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*475-31T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1350-31T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2251-31T>G
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

16-89804354-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804354
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804354
    reference: chr 16
allele count: 4
allele frequency: 3.298479400996141e-5
allele num: 121268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1350-30C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.195-30C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2251-30C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1575-30C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*655G>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1563-30C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*475-30C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*475-30C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*37C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.933-30C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1334-30C>T
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2637
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP

16-89804355-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804355
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804355
    reference: chr 16
allele count: 264
allele frequency: 2.176852798575151e-3
allele num: 121276
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1575-29G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*475-29G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1334-29G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*654C>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.195-29G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*475-29G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.933-29G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*38G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2251-29G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1563-29G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1350-29G>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 5.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 11247
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 13368
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32977
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 2620
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 3
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-89804358-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804358
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804358
    reference: chr 16
allele count: 3
allele frequency: 2.47222863170386e-5
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1563-26C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1334-26C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1575-26C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1350-26C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*475-26C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*41C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*651G>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.195-26C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.933-26C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*475-26C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2251-26C>T
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

16-89804358-CCTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804358
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804355
    reference: chr 16
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2251-22_2251-20delCTT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*475-22_*475-20delCTT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1334-22_1334-20delCTT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*45_*47delCTT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*648_*650delAAG
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.933-22_933-20delCTT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1575-22_1575-20delCTT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1350-22_1350-20delCTT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*475-22_*475-20delCTT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1563-22_1563-20delCTT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.195-22_195-20delCTT
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13427
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: CCTT
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

16-89804364-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804364
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804364
    reference: chr 16
allele count: 1
allele frequency: 8.244159013339049e-6
allele num: 121298
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*475-20T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*645A>G
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1563-20T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*47T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2251-20T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.933-20T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1575-20T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1350-20T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1334-20T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*475-20T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.195-20T>C
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13440
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP

16-89804366-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804366
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804366
    reference: chr 16
allele count: 2
allele frequency: 1.649022129876983e-5
allele num: 121284
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2251-18T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*475-18T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1350-18T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*475-18T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1575-18T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*643A>G
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.933-18T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.195-18T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1334-18T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*49T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1563-18T>C
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33134
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

16-89804366-T-TCTG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804366
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804369
    reference: chr 16
allele count: 4
allele frequency: 3.298044259753966e-5
allele num: 121284
alternate allele: TCTG
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1563-16_1563-14dupTGC
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1575-16_1575-14dupTGC
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.195-16_195-14dupTGC
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1350-16_1350-14dupTGC
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*475-16_*475-14dupTGC
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2251-16_2251-14dupTGC
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*640_*642dupCAG
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.933-16_933-14dupTGC
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*475-16_*475-14dupTGC
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*51_*53dupTGC
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1334-16_1334-14dupTGC
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33134
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11284
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-89804370-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804370
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804370
    reference: chr 16
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.933-14C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1350-14C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1575-14C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.195-14C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*475-14C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*639G>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*53C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1334-14C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*475-14C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1563-14C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2251-14C>T
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13454
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43363
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-89804371-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804371
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804370
    reference: chr 16
allele count: 1
allele frequency: 8.244702778464837e-6
allele num: 121290
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.933-12delT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1350-12delT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1575-12delT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2251-12delT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*55delT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1334-12delT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*637delA
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.195-12delT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1563-12delT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*475-12delT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*475-12delT
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33140
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11265
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: CT
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

16-89804377-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804377
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804377
    reference: chr 16
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1575-7C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1350-7C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*60C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*475-7C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.933-7C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1563-7C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*632G>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.195-7C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*475-7C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2251-7C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1334-7C>T
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1575-7C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-89804380-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804380
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804380
    reference: chr 16
allele count: 1
allele frequency: 8.242256400112095e-6
allele num: 121326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1334-4C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.933-4C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1350-4C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2251-4C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*475-4C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1575-4C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1563-4C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*629G>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*475-4C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.195-4C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*63C>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11246
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1575-4C>A
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum

16-89804390-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804390
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804390
    reference: chr 16
allele count: 5
allele frequency: 4.121128200056047e-5
allele num: 121326
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*619C>G
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.939G>C
  hgvsp: ENSP00000415999.2:p.Glu313Asp
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*73G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1340G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*481G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1569G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1356G>C
  hgvsp: ENSP00000289816.5:p.Glu452Asp
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1581G>C
  hgvsp: ENSP00000415836.2:p.Glu527Asp
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.201G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2257G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*481G>C
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13573
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Glu527Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum

16-89804393-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804393
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804393
    reference: chr 16
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*484C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.204C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2260C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1584C>G
  hgvsp: ENST00000443381.2:c.1584C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*76C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*484C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1572C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.942C>G
  hgvsp: ENST00000446326.2:c.942C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*616G>C
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1359C>G
  hgvsp: ENST00000289816.5:c.1359C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1343C>G
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13576
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val528Val
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-89804401-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804401
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804401
    reference: chr 16
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*84T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1592T>A
  hgvsp: ENSP00000415836.2:p.Phe531Tyr
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.950T>A
  hgvsp: ENSP00000415999.2:p.Phe317Tyr
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.212T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1580T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1367T>A
  hgvsp: ENSP00000289816.5:p.Phe456Tyr
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*492T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*492T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1351T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2268T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*608A>T
  variant of: http://identifiers.org/hgnc/3582
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe531Tyr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-89804401-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804401
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804401
    reference: chr 16
allele count: 2
allele frequency: 1.648532805802836e-5
allele num: 121320
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1351T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1367T>G
  hgvsp: ENSP00000289816.5:p.Phe456Cys
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.212T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.950T>G
  hgvsp: ENSP00000415999.2:p.Phe317Cys
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1580T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*492T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1592T>G
  hgvsp: ENSP00000415836.2:p.Phe531Cys
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*84T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2268T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*608A>C
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*492T>G
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13587
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe531Cys
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

16-89804404-A-ATATTGATTGGGCTGGGGCTGGTCTTGAACTGACTTCATGATCCGCCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804404
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804451
    reference: chr 16
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: ATATTGATTGGGCTGGGGCTGGTCTTGAACTGACTTCATGATCCGCCT
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsp: ENSP00000415836.2:p.Gln532HisfsTer14
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsp: ENSP00000415999.2:p.Gln318HisfsTer14
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsp: ENSP00000289816.5:p.Gln457HisfsTer14
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: stop gained
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33229
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11211
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln532HisfsTer14
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

16-89804411-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804411
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804411
    reference: chr 16
allele count: 2
allele frequency: 1.648723063986942e-5
allele num: 121306
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.222G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*502G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1602G>A
  hgvsp: ENST00000443381.2:c.1602G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1361G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*94G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*502G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1590G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.960G>A
  hgvsp: ENST00000446326.2:c.960G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1377G>A
  hgvsp: ENST00000289816.5:c.1377G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*598C>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2278G>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11203
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg534Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

16-89804414-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804414
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804414
    reference: chr 16
allele count: 1
allele frequency: 8.243207596940122e-6
allele num: 121312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1364G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.225G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*595C>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2281G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.963G>A
  hgvsp: ENST00000446326.2:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*97G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1380G>A
  hgvsp: ENST00000289816.5:c.1380G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1605G>A
  hgvsp: ENST00000443381.2:c.1605G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*505G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*505G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1593G>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11192
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln535Gln
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

16-89804415-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804415
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804415
    reference: chr 16
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1381C>T
  hgvsp: ENSP00000289816.5:p.Arg461Trp
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*506C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2282C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*98C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.964C>T
  hgvsp: ENSP00000415999.2:p.Arg322Trp
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.226C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1606C>T
  hgvsp: ENSP00000415836.2:p.Arg536Trp
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1594C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*594G>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*506C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1365C>T
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33233
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13594
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg536Trp
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-89804436-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804436
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804436
    reference: chr 16
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.247A>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.985A>C
  hgvsp: ENSP00000415999.2:p.Met329Leu
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1386A>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*527A>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*527A>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2303A>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1402A>C
  hgvsp: ENSP00000289816.5:p.Met468Leu
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1627A>C
  hgvsp: ENSP00000415836.2:p.Met543Leu
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*119A>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*573T>G
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1615A>C
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met543Leu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

16-89804436-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804436
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804436
    reference: chr 16
allele count: 1
allele frequency: 8.247014580721778e-6
allele num: 121256
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2303A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*527A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*119A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.985A>G
  hgvsp: ENSP00000415999.2:p.Met329Val
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*527A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.247A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1615A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1402A>G
  hgvsp: ENSP00000289816.5:p.Met468Val
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*573T>C
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1627A>G
  hgvsp: ENSP00000415836.2:p.Met543Val
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1386A>G
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33236
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met543Val
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

16-89804441-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804441
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804441
    reference: chr 16
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1632C>T
  hgvsp: ENST00000443381.2:c.1632C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2308C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.252C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*124C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*532C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.990C>T
  hgvsp: ENST00000446326.2:c.990C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1407C>T
  hgvsp: ENST00000289816.5:c.1407C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*568G>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1391C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1620C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*532C>T
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr544Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

16-89804450-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804450
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804450
    reference: chr 16
allele count: 3
allele frequency: 2.475288371095233e-5
allele num: 121198
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*559C>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1641G>A
  hgvsp: ENST00000443381.2:c.1641G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*133G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.999G>A
  hgvsp: ENST00000446326.2:c.999G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2317G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1416G>A
  hgvsp: ENST00000289816.5:c.1416G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*541G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.261G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*541G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1400G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1629G>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13652
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33197
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys547Lys
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: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

16-89804457-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804457
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804457
    reference: chr 16
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2324A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*548A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*140A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*548A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.268A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1423A>G
  hgvsp: ENSP00000289816.5:p.Thr475Ala
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1648A>G
  hgvsp: ENSP00000415836.2:p.Thr550Ala
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1407A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1006A>G
  hgvsp: ENSP00000415999.2:p.Thr336Ala
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1636A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*552T>C
  variant of: http://identifiers.org/hgnc/3582
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33169
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr550Ala
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: A
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum

16-89804471-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804471
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804471
    reference: chr 16
allele count: 1
allele frequency: 8.257365570088519e-6
allele num: 121104
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1650T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*562T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1437T>C
  hgvsp: ENST00000289816.5:c.1437T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*562T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*538A>G
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1662T>C
  hgvsp: ENST00000443381.2:c.1662T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*154T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1020T>C
  hgvsp: ENST00000446326.2:c.1020T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2338T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.282T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1421T>C
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11009
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe554Phe
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

16-89804474-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804474
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804474
    reference: chr 16
allele count: 1
allele frequency: 8.259684480052863e-6
allele num: 121070
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2341C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1440C>G
  hgvsp: ENST00000289816.5:c.1440C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*565C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1665C>G
  hgvsp: ENST00000443381.2:c.1665C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1023C>G
  hgvsp: ENST00000446326.2:c.1023C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*535G>C
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1424C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.285C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1653C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*157C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*565C>G
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13770
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33143
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala555Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

16-89804477-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804477
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804477
    reference: chr 16
allele count: 1
allele frequency: 8.26255081468751e-6
allele num: 121028
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1668T>C
  hgvsp: ENST00000443381.2:c.1668T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2344T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1443T>C
  hgvsp: ENST00000289816.5:c.1443T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*160T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*568T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1427T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*532A>G
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1026T>C
  hgvsp: ENST00000446326.2:c.1026T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*568T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.288T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1656T>C
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13775
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10967
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys556Cys
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

16-89804478-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804478
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804478
    reference: chr 16
allele count: 1
allele frequency: 8.263916435277007e-6
allele num: 121008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.289G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1669G>A
  hgvsp: ENSP00000415836.2:p.Asp557Asn
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*569G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1428G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1444G>A
  hgvsp: ENSP00000289816.5:p.Asp482Asn
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*569G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*531C>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2345G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*161G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1027G>A
  hgvsp: ENSP00000415999.2:p.Asp343Asn
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1657G>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp557Asn
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: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

16-89804480-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804480
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804480
    reference: chr 16
allele count: 1
allele frequency: 8.266375690242371e-6
allele num: 120972
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1029C>G
  hgvsp: ENSP00000415999.2:p.Asp343Glu
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1659C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1671C>G
  hgvsp: ENSP00000415836.2:p.Asp557Glu
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*571C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*571C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1430C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2347C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1446C>G
  hgvsp: ENSP00000289816.5:p.Asp482Glu
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*163C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*529G>C
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.291C>G
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp557Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

16-89804480-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804480
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804480
    reference: chr 16
allele count: 1
allele frequency: 8.266375690242371e-6
allele num: 120972
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1430C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.291C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*571C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1029C>T
  hgvsp: ENST00000446326.2:c.1029C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1659C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2347C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*529G>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1671C>T
  hgvsp: ENST00000443381.2:c.1671C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1446C>T
  hgvsp: ENST00000289816.5:c.1446C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*571C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*163C>T
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13770
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp557Asp
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

16-89804481-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804481
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804481
    reference: chr 16
allele count: 1
allele frequency: 8.267469162340024e-6
allele num: 120956
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*164C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2348C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1447C>T
  hgvsp: ENSP00000289816.5:p.Gln483Ter
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*572C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*528G>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1672C>T
  hgvsp: ENSP00000415836.2:p.Gln558Ter
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1030C>T
  hgvsp: ENSP00000415999.2:p.Gln344Ter
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.292C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*572C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1660C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1431C>T
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln558Ter
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

16-89804483-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804483
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804483
    reference: chr 16
allele count: 1
allele frequency: 8.269246671628215e-6
allele num: 120930
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1449G>C
  hgvsp: ENSP00000289816.5:p.Gln483His
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1674G>C
  hgvsp: ENSP00000415836.2:p.Gln558His
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1032G>C
  hgvsp: ENSP00000415999.2:p.Gln344His
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*166G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*574G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2350G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1433G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1662G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.294G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*526C>G
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*574G>C
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13786
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10920
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln558His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

16-89804488-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804488
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804488
    reference: chr 16
allele count: 54
allele frequency: 4.469532685526991e-4
allele num: 120818
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*579G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1454G>A
  hgvsp: ENSP00000289816.5:p.Gly485Asp
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*521C>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*579G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1438G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1667G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1037G>A
  hgvsp: ENSP00000415999.2:p.Gly346Asp
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1679G>A
  hgvsp: ENSP00000415836.2:p.Gly560Asp
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*171G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.299G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2355G>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32926
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10857
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13832
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
hgvs: p.Gly560Asp
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD

16-89804490-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804490
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804490
    reference: chr 16
allele count: 1
allele frequency: 8.279242283746192e-6
allele num: 120784
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1681C>T
  hgvsp: ENSP00000415836.2:p.Arg561Trp
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*581C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*581C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1039C>T
  hgvsp: ENSP00000415999.2:p.Arg347Trp
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1440C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*519G>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.301C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1669C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*173C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1456C>T
  hgvsp: ENSP00000289816.5:p.Arg486Trp
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2357C>T
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10812
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg561Trp
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

16-89804493-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804493
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804493
    reference: chr 16
allele count: 1
allele frequency: 8.285004142502071e-6
allele num: 120700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.304C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1684C>T
  hgvsp: ENSP00000415836.2:p.Arg562Trp
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2360C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*584C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*516G>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*584C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*176C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1443C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1672C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1459C>T
  hgvsp: ENSP00000289816.5:p.Arg487Trp
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1042C>T
  hgvsp: ENSP00000415999.2:p.Arg348Trp
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13979
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg562Trp
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

16-89804494-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804494
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804494
    reference: chr 16
allele count: 5
allele frequency: 4.144150117693863e-5
allele num: 120652
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*585G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*515C>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*177G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1685G>A
  hgvsp: ENSP00000415836.2:p.Arg562Gln
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1460G>A
  hgvsp: ENSP00000289816.5:p.Arg487Gln
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1444G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1673G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*585G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1043G>A
  hgvsp: ENSP00000415999.2:p.Arg348Gln
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.305G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2361G>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10654
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg562Gln
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

16-89804500-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804500
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804499
    reference: chr 16
allele count: 1
allele frequency: 8.291048983517394e-6
allele num: 120612
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1680delG
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*592delG
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.312delG
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1467delG
  hgvsp: ENSP00000289816.5:p.Lys490ArgfsTer15
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1451delG
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*592delG
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1692delG
  hgvsp: ENSP00000415836.2:p.Lys565ArgfsTer15
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2368delG
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*184delG
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1050delG
  hgvsp: ENSP00000415999.2:p.Lys351ArgfsTer15
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*508delC
  variant of: http://identifiers.org/hgnc/3582
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10540
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32828
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys565ArgfsTer15
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: AG
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

16-89804502-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804502
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804502
    reference: chr 16
allele count: 2
allele frequency: 1.658897496723677e-5
allele num: 120562
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*593A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*593A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1693A>G
  hgvsp: ENSP00000415836.2:p.Lys565Glu
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*507T>C
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2369A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1468A>G
  hgvsp: ENSP00000289816.5:p.Lys490Glu
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1051A>G
  hgvsp: ENSP00000415999.2:p.Lys351Glu
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1452A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1681A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.313A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*185A>G
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys565Glu
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

16-89804521-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804521
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804521
    reference: chr 16
allele count: 1
allele frequency: 8.343484572897024e-6
allele num: 119854
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2388T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1712T>G
  hgvsp: ENSP00000415836.2:p.Val571Gly
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.332T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*612T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1700T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1471T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*612T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1070T>G
  hgvsp: ENSP00000415999.2:p.Val357Gly
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*204T>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1487T>G
  hgvsp: ENSP00000289816.5:p.Val496Gly
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*488A>C
  variant of: http://identifiers.org/hgnc/3582
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 32194
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14368
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val571Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD

16-89804525-CAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804525
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804523
    reference: chr 16
allele count: 2
allele frequency: 1.672744304305644e-5
allele num: 119564
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1476_1477delAT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1492_1493delAT
  hgvsp: ENSP00000289816.5:p.Met498ValfsTer107
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2393_2394delAT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.337_338delAT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1717_1718delAT
  hgvsp: ENSP00000415836.2:p.Met573ValfsTer107
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*209_*210delAT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*482_*483delAT
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*617_*618delAT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*617_*618delAT
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1075_1076delAT
  hgvsp: ENSP00000415999.2:p.Met359ValfsTer?
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1705_1706delAT
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10059
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1028
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met573ValfsTer107
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: CAT
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP

16-89804527-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804527
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804527
    reference: chr 16
allele count: 1
allele frequency: 8.378437253883405e-6
allele num: 119354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1493T>A
  hgvsp: ENSP00000289816.5:p.Met498Lys
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1718T>A
  hgvsp: ENSP00000415836.2:p.Met573Lys
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*482A>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2394T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1706T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*210T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1076T>A
  hgvsp: ENSP00000415999.2:p.Met359Lys
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.338T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*618T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*618T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1477T>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31739
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9992
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met573Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-89804530-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804530
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804530
    reference: chr 16
allele count: 1
allele frequency: 8.396869646995599e-6
allele num: 119092
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1721C>A
  hgvsp: ENSP00000415836.2:p.Ser574Tyr
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1079C>A
  hgvsp: ENSP00000415999.2:p.Ser360Tyr
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1480C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1709C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*213C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1496C>A
  hgvsp: ENSP00000289816.5:p.Ser499Tyr
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*621C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*479G>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2397C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*621C>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.341C>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14249
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31426
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser574Tyr
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

16-89804532-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804532
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804532
    reference: chr 16
allele count: 3
allele frequency: 2.519314746388982e-5
allele num: 119080
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1482A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*215A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*477T>C
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1498A>G
  hgvsp: ENSP00000289816.5:p.Met500Val
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.343A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1081A>G
  hgvsp: ENSP00000415999.2:p.Met361Val
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2399A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1723A>G
  hgvsp: ENSP00000415836.2:p.Met575Val
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*623A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1711A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*623A>G
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31409
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9807
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met575Val
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS

16-89804534-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804534
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804534
    reference: chr 16
allele count: 9
allele frequency: 7.577288341079006e-5
allele num: 118776
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1083G>C
  hgvsp: ENSP00000415999.2:p.Met361Ile
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1725G>C
  hgvsp: ENSP00000415836.2:p.Met575Ile
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*625G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*475C>G
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2401G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*217G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1500G>C
  hgvsp: ENSP00000289816.5:p.Met500Ile
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1713G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*625G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1484G>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.345G>C
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31089
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9741
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14373
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met575Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

16-89804538-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804538
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804538
    reference: chr 16
allele count: 1
allele frequency: 8.459664320519762e-6
allele num: 118208
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1504C>T
  hgvsp: ENSP00000289816.5:p.His502Tyr
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*629C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1488C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1729C>T
  hgvsp: ENSP00000415836.2:p.His577Tyr
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*471G>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1087C>T
  hgvsp: ENSP00000415999.2:p.His363Tyr
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.349C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*221C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*629C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1717C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2405C>T
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14569
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His577Tyr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

16-89804541-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804541
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804541
    reference: chr 16
allele count: 1
allele frequency: 8.463530646444471e-6
allele num: 118154
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1732C>G
  hgvsp: ENSP00000415836.2:p.Pro578Ala
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1090C>G
  hgvsp: ENSP00000415999.2:p.Pro364Ala
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2408C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*224C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1507C>G
  hgvsp: ENSP00000289816.5:p.Pro503Ala
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*468G>C
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.352C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*632C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*632C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1491C>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1720C>G
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30348
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9311
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro578Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
reference allele: C
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-89804542-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804542
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804542
    reference: chr 16
allele count: 3
allele frequency: 2.543580004069728e-5
allele num: 117944
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1091C>T
  hgvsp: ENSP00000415999.2:p.Pro364Leu
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2409C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*225C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1733C>T
  hgvsp: ENSP00000415836.2:p.Pro578Leu
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*467G>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1721C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.353C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1492C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1508C>T
  hgvsp: ENSP00000289816.5:p.Pro503Leu
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*633C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*633C>T
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1596
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9284
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro578Leu
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: MQ

16-89804543-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804543
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804543
    reference: chr 16
allele count: 5
allele frequency: 4.242753377231689e-5
allele num: 117848
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*634G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*634G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1092G>A
  hgvsp: ENST00000446326.2:c.1092G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.354G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*226G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1734G>A
  hgvsp: ENST00000443381.2:c.1734G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*466C>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1509G>A
  hgvsp: ENST00000289816.5:c.1509G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2410G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1493G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1722G>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9184
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro578Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

16-89804545-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804545
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804545
    reference: chr 16
allele count: 1
allele frequency: 8.497909514259493e-6
allele num: 117676
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1736T>A
  hgvsp: ENSP00000415836.2:p.Leu579Gln
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*636T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*464A>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.356T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*228T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2412T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1511T>A
  hgvsp: ENSP00000289816.5:p.Leu504Gln
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1724T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1094T>A
  hgvsp: ENSP00000415999.2:p.Leu365Gln
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1495T>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*636T>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15142
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu579Gln
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

16-89804546-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804546
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804546
    reference: chr 16
allele count: 3
allele frequency: 2.553017666882255e-5
allele num: 117508
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*637G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1512G>A
  hgvsp: ENST00000289816.5:c.1512G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*229G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1095G>A
  hgvsp: ENST00000446326.2:c.1095G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2413G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1725G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1737G>A
  hgvsp: ENST00000443381.2:c.1737G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1496G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*637G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*463C>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.357G>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29800
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9007
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu579Leu
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

16-89804558-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804558
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804558
    reference: chr 16
allele count: 2
allele frequency: 1.735538624412086e-5
allele num: 115238
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*451C>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1524G>A
  hgvsp: ENST00000289816.5:c.1524G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.369G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1749G>A
  hgvsp: ENST00000443381.2:c.1749G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1508G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*649G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1107G>A
  hgvsp: ENST00000446326.2:c.1107G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*241G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2425G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*649G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1737G>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8440
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln583Gln
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

16-89804559-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804559
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804559
    reference: chr 16
allele count: 1
allele frequency: 8.701251239928301e-6
allele num: 114926
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1738G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*242G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*450C>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1525G>A
  hgvsp: ENSP00000289816.5:p.Asp509Asn
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2426G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1750G>A
  hgvsp: ENSP00000415836.2:p.Asp584Asn
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*650G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.370G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*650G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1108G>A
  hgvsp: ENSP00000415999.2:p.Asp370Asn
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1509G>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp584Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

16-89804559-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804559
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804559
    reference: chr 16
allele count: 3
allele frequency: 2.610375371978491e-5
allele num: 114926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*650G>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1738G>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*650G>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1525G>T
  hgvsp: ENSP00000289816.5:p.Asp509Tyr
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1108G>T
  hgvsp: ENSP00000415999.2:p.Asp370Tyr
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1750G>T
  hgvsp: ENSP00000415836.2:p.Asp584Tyr
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*450C>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2426G>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*242G>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1509G>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.370G>T
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27947
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8362
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1447
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp584Tyr
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ

16-89804560-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804560
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804560
    reference: chr 16
allele count: 3
allele frequency: 2.623386617230403e-5
allele num: 114356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*651A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1526A>G
  hgvsp: ENSP00000289816.5:p.Asp509Gly
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2427A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1751A>G
  hgvsp: ENSP00000415836.2:p.Asp584Gly
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*651A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*449T>C
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.371A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*243A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1109A>G
  hgvsp: ENSP00000415999.2:p.Asp370Gly
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1510A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1739A>G
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13810
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp584Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: MQ

16-89804562-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804562
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804562
    reference: chr 16
allele count: 3
allele frequency: 2.635555399374495e-5
allele num: 113828
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*245A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1512A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1741A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.373A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*653A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*653A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1753A>G
  hgvsp: ENSP00000415836.2:p.Lys585Glu
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1528A>G
  hgvsp: ENSP00000289816.5:p.Lys510Glu
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2429A>G
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*447T>C
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1111A>G
  hgvsp: ENSP00000415999.2:p.Lys371Glu
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26973
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8127
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13676
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3568
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1746
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys585Glu
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

16-89804563-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804563
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804563
    reference: chr 16
allele count: 45
allele frequency: 3.962244215123446e-4
allele num: 113572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1112A>T
  hgvsp: ENSP00000415999.2:p.Lys371Met
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1754A>T
  hgvsp: ENSP00000415836.2:p.Lys585Met
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2430A>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1529A>T
  hgvsp: ENSP00000289816.5:p.Lys510Met
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1742A>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*654A>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*654A>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*246A>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*446T>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.374A>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1513A>T
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26759
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5163
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3680
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8062
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 13596
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 1.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
hgvs: p.Lys585Met
num of homozygotes: 1
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-89804572-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804572
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804572
    reference: chr 16
allele count: 4
allele frequency: 3.678769819372402e-5
allele num: 108732
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1522C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*255C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1763C>T
  hgvsp: ENSP00000415836.2:p.Pro588Leu
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*437G>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.383C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2439C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*663C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1121C>T
  hgvsp: ENSP00000415999.2:p.Pro374Leu
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1538C>T
  hgvsp: ENSP00000289816.5:p.Pro513Leu
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*663C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1751C>T
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5933
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6308
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12594
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8415
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro588Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

16-89804575-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804575
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804575
    reference: chr 16
allele count: 1
allele frequency: 9.340382208439969e-6
allele num: 107062
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1124T>C
  hgvsp: ENSP00000415999.2:p.Leu375Pro
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*666T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*258T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*434A>G
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1766T>C
  hgvsp: ENSP00000415836.2:p.Leu589Pro
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1754T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2442T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1541T>C
  hgvsp: ENSP00000289816.5:p.Leu514Pro
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*666T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.386T>C
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1525T>C
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6644
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12604
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9306
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21011
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3955
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu589Pro
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
reference allele: T
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

16-89804577-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804577
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804577
    reference: chr 16
allele count: 1
allele frequency: 9.42560370991762e-6
allele num: 106094
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*260G>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*668G>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1768G>T
  hgvsp: ENSP00000415836.2:p.Glu590Ter
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.388G>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1543G>T
  hgvsp: ENSP00000289816.5:p.Glu515Ter
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1527G>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1126G>T
  hgvsp: ENSP00000415999.2:p.Glu376Ter
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*432C>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*668G>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2444G>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1756G>T
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu590Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff

16-89804581-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804581
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804581
    reference: chr 16
allele count: 4
allele frequency: 3.843714565756347e-5
allele num: 104066
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*428G>A
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1531C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1547C>T
  hgvsp: ENSP00000289816.5:p.Ala516Val
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.392C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1130C>T
  hgvsp: ENSP00000415999.2:p.Ala377Val
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*672C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1760C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2448C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1772C>T
  hgvsp: ENSP00000415836.2:p.Ala591Val
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*264C>T
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*672C>T
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18155
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7924
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5019
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala591Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

16-89804582-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 89804582
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 89804582
    reference: chr 16
allele count: 6
allele frequency: 5.798670171640637e-5
allele num: 103472
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000563983
  gene symbol: ZNF276
  hgvsc: ENST00000563983.1:n.1761G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000564004
  gene symbol: ZNF276
  hgvsc: ENST00000564004.1:n.2449G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457313
  ensembl transcript: ENST00000568295
  gene symbol: ZNF276
  hgvsc: ENST00000568295.1:c.*673G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415836
  ensembl transcript: ENST00000443381
  gene symbol: ZNF276
  hgvsc: ENST00000443381.2:c.1773G>A
  hgvsp: ENST00000443381.2:c.1773G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000455466
  ensembl transcript: ENST00000562530
  gene symbol: ZNF276
  hgvsc: ENST00000562530.1:c.*673G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000289816
  ensembl transcript: ENST00000289816
  gene symbol: ZNF276
  hgvsc: ENST00000289816.5:c.1548G>A
  hgvsp: ENST00000289816.5:c.1548G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000569901
  gene symbol: ZNF276
  hgvsc: ENST00000569901.1:n.393G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000187741
  ensembl protein: ENSP00000373952
  ensembl transcript: ENST00000389301
  gene symbol: FANCA
  hgvsc: ENST00000389301.3:c.*427C>T
  variant of: http://identifiers.org/hgnc/3582
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000457210
  ensembl transcript: ENST00000568064
  gene symbol: ZNF276
  hgvsc: ENST00000568064.1:c.*265G>A
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000158805
  ensembl protein: ENSP00000415999
  ensembl transcript: ENST00000446326
  gene symbol: ZNF276
  hgvsc: ENST00000446326.2:c.1131G>A
  hgvsp: ENST00000446326.2:c.1131G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23330
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000158805
  ensembl transcript: ENST00000561536
  gene symbol: ZNF276
  hgvsc: ENST00000561536.1:n.1532G>A
  variant of: http://identifiers.org/hgnc/23330
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5084
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17757
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4475
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10851
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala591Ala
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 22
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9284
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2536
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40917
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1483
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 322
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1529
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2307
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65328
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13838
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.712509712509713e-5
allele num: 10296
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6448
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.801484e6

VQSLOD
type: SiteQuality
SIO_000300: -1.261e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.31e-1

FS
type: SiteQuality
SIO_000300: 2.716e0

MQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

MQ
type: SiteQuality
SIO_000300: 6.122e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.606e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

QD
type: SiteQuality
SIO_000300: 1.652e1

GenotypeQuality
all individuals: 9638
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2393
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2605
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42575
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1435
bin: 9.75e1
variant carriers: 641

GenotypeQuality
all individuals: 1013
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 31
allele frequency: 2.682589131187262e-3
allele num: 11556
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

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

African
type: Population
allele count: 620
allele frequency: 5.978784956605593e-2
allele num: 10370
num of homozygotes: 22

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.65026404224676e-4
allele num: 66656
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 2.028e1

MQ
type: SiteQuality
SIO_000300: 5.983e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.69e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.24e-1

DP
type: SiteQuality
SIO_000300: 1.706873e6

VQSLOD
type: SiteQuality
SIO_000300: 4.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.592e0

GenotypeQuality
all individuals: 52
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42575
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2605
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9638
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1435
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2393
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1013
bin: 8.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 2.028e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.69e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.592e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.5e0

DP
type: SiteQuality
SIO_000300: 1.706873e6

MQ
type: SiteQuality
SIO_000300: 5.983e1

MQRankSum
type: SiteQuality
SIO_000300: 4.24e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2657
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1021
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 9.75e1
variant carriers: 2

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

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

GenotypeQuality
all individuals: 48
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2413
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9768
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43105
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499925003749813e-5
allele num: 66670
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 7.11e0

VQSLOD
type: SiteQuality
SIO_000300: -1.351e0

QD
type: SiteQuality
SIO_000300: 2.447e1

DP
type: SiteQuality
SIO_000300: 1.676435e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.307e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.73e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.78e-1

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

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

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1020
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9770
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43053
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2650
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 47
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 305
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

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

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

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

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

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

DP
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ClippingRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 5.148e0

MQRankSum
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VQSLOD
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QD
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.278e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.98e-1

MQ
type: SiteQuality
SIO_000300: 6.014e1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

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

African
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allele frequency: 0.0e0
allele num: 10388
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
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500105007350515e-5
allele num: 66662
num of homozygotes: 0

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

InbreedingCoeff
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ClippingRankSum
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DP
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VQSLOD
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SIO_000300: -3.897e-1

FS
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SIO_000300: 4.103e0

MQRankSum
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SIO_000300: 3.43e-1

BaseQRankSum
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SIO_000300: -2.082e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

MQ
type: SiteQuality
SIO_000300: 6.023e1

QD
type: SiteQuality
SIO_000300: 1.822e1

GenotypeQuality
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 6.016e1

DP
type: SiteQuality
SIO_000300: 1.674263e6

MQRankSum
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SIO_000300: 1.1e0

InbreedingCoeff
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SIO_000300: 2.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

FS
type: SiteQuality
SIO_000300: 2.212e0

VQSLOD
type: SiteQuality
SIO_000300: 5.600000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 1.25e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
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: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.593809441466367e-4
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.36e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.089e0

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.88e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.59e-1

FS
type: SiteQuality
SIO_000300: 1.196e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.674331e6

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 902
bin: 9.75e1
variant carriers: 260

Latino
type: Population
allele count: 18
allele frequency: 1.556016597510373e-3
allele num: 11568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 238
allele frequency: 3.569393203155464e-3
allele num: 66678
num of homozygotes: 3

African
type: Population
allele count: 1
allele frequency: 9.626492106276473e-5
allele num: 10388
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.029201502483945e-4
allele num: 16506
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.207505518763797e-3
allele num: 906
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.17e-1

VQSLOD
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MQRankSum
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MQ
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DP
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BaseQRankSum
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SIO_000300: 1.17e-1

QD
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.29e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.32e-1

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

ClippingRankSum
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SIO_000300: 2.6e-1

BaseQRankSum
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DP
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QD
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FS
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VQSLOD
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 906
num of homozygotes: 0

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

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

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

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

African
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South Asian
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VQSLOD
type: SiteQuality
SIO_000300: 1.57e0

ReadPosRankSum
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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FS
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MQ
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

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

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

African
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allele count: 0
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.86e-1

MQ
type: SiteQuality
SIO_000300: 6.042e1

ReadPosRankSum
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BaseQRankSum
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VQSLOD
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QD
type: SiteQuality
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MQRankSum
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FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 5.4e-3

DP
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SIO_000300: 1.66679e6

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43350
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2625
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 16
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9760
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2380
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.92492781520693e-4
allele num: 10390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.555e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

FS
type: SiteQuality
SIO_000300: 1.335e0

QD
type: SiteQuality
SIO_000300: 1.474e1

DP
type: SiteQuality
SIO_000300: 1.666548e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

MQ
type: SiteQuality
SIO_000300: 5.634e1

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

GenotypeQuality
all individuals: 2380
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 995
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.42306760358614e-4
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.31e0

MQRankSum
type: SiteQuality
SIO_000300: -1.555e0

FS
type: SiteQuality
SIO_000300: 1.335e0

DP
type: SiteQuality
SIO_000300: 1.666548e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

QD
type: SiteQuality
SIO_000300: 1.474e1

MQ
type: SiteQuality
SIO_000300: 5.634e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.9e-1

GenotypeQuality
all individuals: 991
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2380
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2615
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 267
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variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
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GenotypeQuality
all individuals: 42
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 666
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variant carriers: 1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9758
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.723e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.704e0

MQ
type: SiteQuality
SIO_000300: 6.062e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

FS
type: SiteQuality
SIO_000300: 5.158e0

DP
type: SiteQuality
SIO_000300: 1.665641e6

QD
type: SiteQuality
SIO_000300: 1.504e1

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.895e0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2379
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variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 986
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2616
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.665553e6

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.208e0

VQSLOD
type: SiteQuality
SIO_000300: 5.34e0

QD
type: SiteQuality
SIO_000300: 1.192e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.961e1

GenotypeDepth
all individuals: 68
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2605
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 43485
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 981
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

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

GenotypeQuality
all individuals: 9752
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

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

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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.017e1

VQSLOD
type: SiteQuality
SIO_000300: -1.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.981e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

FS
type: SiteQuality
SIO_000300: 5.973e0

MQ
type: SiteQuality
SIO_000300: 6.09e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.21e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.22e-1

DP
type: SiteQuality
SIO_000300: 1.664186e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.1e-2

DP
type: SiteQuality
SIO_000300: 1.663646e6

FS
type: SiteQuality
SIO_000300: 3.116e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 7.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.121e0

VQSLOD
type: SiteQuality
SIO_000300: -9.094e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.76e-1

MQ
type: SiteQuality
SIO_000300: 6.043e1

MQRankSum
type: SiteQuality
SIO_000300: -5.44e-1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 611
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variant carriers: 5

GenotypeQuality
all individuals: 273
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variant carriers: 0

GenotypeQuality
all individuals: 2591
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 5
allele frequency: 5.780346820809249e-4
allele num: 8650
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 1.662243e6

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.078e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.684e0

MQRankSum
type: SiteQuality
SIO_000300: 4.67e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 21
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variant carriers: 0

GenotypeQuality
all individuals: 2366
bin: 7.75e1
variant carriers: 0

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QD
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DP
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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VQSLOD
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MQ
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QD
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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East Asian
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European (Finnish)
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South Asian
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MQRankSum
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VQSLOD
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DP
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MQ
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BaseQRankSum
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Latino
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East Asian
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South Asian
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BaseQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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DP
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MQ
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ClippingRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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European (Non-Finnish)
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African
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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VQSLOD
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FS
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MQ
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QD
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South Asian
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European (Finnish)
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East Asian
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InbreedingCoeff
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QD
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VQSLOD
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MQ
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FS
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European (Non-Finnish)
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African
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East Asian
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FS
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MQ
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DP
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QD
type: SiteQuality
SIO_000300: 1.247e1

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

GenotypeQuality
all individuals: 32
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 243
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 947
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43750
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9694
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2553
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2335
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 591
bin: 9.75e1
variant carriers: 1

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

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

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.81e-1

FS
type: SiteQuality
SIO_000300: 7.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.09e-1

QD
type: SiteQuality
SIO_000300: 1.247e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 1.659257e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 946
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9684
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2545
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43736
bin: 6.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.978e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
SIO_000300: 1.65901e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.01e-1

FS
type: SiteQuality
SIO_000300: 1.631e0

VQSLOD
type: SiteQuality
SIO_000300: 5.46e-1

QD
type: SiteQuality
SIO_000300: 1.27e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

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

GenotypeQuality
all individuals: 939
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 584
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 240
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2323
bin: 7.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.644536652835408e-5
allele num: 11568
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.00336376741951e-5
allele num: 66592
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.28e1

MQRankSum
type: SiteQuality
SIO_000300: -1.047e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.533e0

DP
type: SiteQuality
SIO_000300: 1.657598e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-2

FS
type: SiteQuality
SIO_000300: 4.97e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2307
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2530
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43621
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 933
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 578
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 237
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variant carriers: 0

GenotypeQuality
all individuals: 262
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variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9660
bin: 6.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501862309263487e-5
allele num: 66584
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.510000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.139999999999999e-1

QD
type: SiteQuality
SIO_000300: 2.753e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e0

MQRankSum
type: SiteQuality
SIO_000300: -2.38e-1

FS
type: SiteQuality
SIO_000300: 4.453e0

DP
type: SiteQuality
SIO_000300: 1.656237e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e-1

GenotypeQuality
all individuals: 61
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2518
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 917
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variant carriers: 0

GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 572
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 265
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2287
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43759
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9631
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50271992306074e-5
allele num: 66546
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 6.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.4e-1

DP
type: SiteQuality
SIO_000300: 1.654271e6

QD
type: SiteQuality
SIO_000300: 1.336e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.976e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.91e0

MQRankSum
type: SiteQuality
SIO_000300: -1.108e0

VQSLOD
type: SiteQuality
SIO_000300: 4.69e-1

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

GenotypeQuality
all individuals: 281
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variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 2271
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 565
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variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 43782
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9610
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2500
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.653231e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.91e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.97e-1

QD
type: SiteQuality
SIO_000300: 1.664e1

MQ
type: SiteQuality
SIO_000300: 5.903e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.281e0

MQRankSum
type: SiteQuality
SIO_000300: 2.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e-1

GenotypeQuality
all individuals: 9567
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 43743
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 907
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variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 309
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66506
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.737e1

DP
type: SiteQuality
SIO_000300: 1.652072e6

MQ
type: SiteQuality
SIO_000300: 5.899e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.569e0

MQRankSum
type: SiteQuality
SIO_000300: -9.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

VQSLOD
type: SiteQuality
SIO_000300: -9.84e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
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variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43691
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

Other
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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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allele frequency: 0.0e0
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African
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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BaseQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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MQ
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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FS
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SIO_000300: 6.805e0

QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.504347564461293e-5
allele num: 66474
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Latino
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Other
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African
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allele frequency: 0.0e0
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South Asian
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ReadPosRankSum
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VQSLOD
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FS
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MQRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 8644
num of homozygotes: 0

African
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Latino
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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BaseQRankSum
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ClippingRankSum
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QD
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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InbreedingCoeff
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66464
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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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Other
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ClippingRankSum
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DP
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QD
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ReadPosRankSum
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MQ
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VQSLOD
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MQRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele num: 8638
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African
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Other
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European (Finnish)
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South Asian
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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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DP
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MQ
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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allele frequency: 7.804370447450572e-4
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European (Non-Finnish)
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allele num: 66382
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East Asian
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African
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Other
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South Asian
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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FS
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VQSLOD
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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African
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European (Finnish)
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Latino
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East Asian
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ReadPosRankSum
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DP
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InbreedingCoeff
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FS
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MQRankSum
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MQ
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VQSLOD
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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South Asian
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African
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European (Finnish)
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Other
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Latino
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FS
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -4.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

VQSLOD
type: SiteQuality
SIO_000300: 9.1e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

QD
type: SiteQuality
SIO_000300: 1.392e1

DP
type: SiteQuality
SIO_000300: 1.641072e6

GenotypeQuality
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variant carriers: 0

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.735207357279195e-4
allele num: 11526
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.526662039412137e-5
allele num: 66274
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 2.4e-1

MQRankSum
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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SIO_000300: -1.68e-1

QD
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SIO_000300: 1.331e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.638919e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 894
num of homozygotes: 0

South Asian
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: 8630
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.509661835748792e-5
allele num: 66240
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

ClippingRankSum
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DP
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SIO_000300: 1.634336e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.052e1

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

ReadPosRankSum
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SIO_000300: -6.860000000000001e-1

BaseQRankSum
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SIO_000300: -1.376e0

VQSLOD
type: SiteQuality
SIO_000300: 3.83e0

MQ
type: SiteQuality
SIO_000300: 6.104e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66206
num of homozygotes: 0

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

South Asian
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allele count: 2
allele frequency: 1.21256214380987e-4
allele num: 16494
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 1.63294e6

FS
type: SiteQuality
SIO_000300: 2.856e0

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

ClippingRankSum
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SIO_000300: 1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e0

VQSLOD
type: SiteQuality
SIO_000300: 6.95e-1

QD
type: SiteQuality
SIO_000300: 1.057e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.2e-3

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.520542529574552e-5
allele num: 65766
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

ClippingRankSum
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FS
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SIO_000300: 0.0e0

BaseQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: -2.742e0

InbreedingCoeff
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SIO_000300: -4.0e-4

ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.816e1

DP
type: SiteQuality
SIO_000300: 1.614113e6

QD
type: SiteQuality
SIO_000300: 1.275e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.164144353899884e-4
allele num: 8590
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 878
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6368
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.524436720631727e-5
allele num: 65598
num of homozygotes: 0

MQRankSum
type: SiteQuality
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QD
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InbreedingCoeff
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SIO_000300: -5.0e-4

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16420
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11446
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8582
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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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.526857422053929e-5
allele num: 65494
num of homozygotes: 0

Other
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QD
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SIO_000300: 1.313e1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

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
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.76731544800982e-5
allele num: 11406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65356
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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QD
type: SiteQuality
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VQSLOD
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MQRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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MQ
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ClippingRankSum
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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

Latino
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allele frequency: 0.0e0
allele num: 11410
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 3.060818462856968e-5
allele num: 65342
num of homozygotes: 0

European (Finnish)
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allele frequency: 1.580278128950695e-4
allele num: 6328
num of homozygotes: 0

Other
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BaseQRankSum
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SIO_000300: 2.34e0

ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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MQRankSum
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DP
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MQ
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
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SIO_000300: 6.99e-1

FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

African
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allele frequency: 0.0e0
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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

European (Non-Finnish)
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allele count: 9
allele frequency: 1.380961148959676e-4
allele num: 65172
num of homozygotes: 0

Other
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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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ReadPosRankSum
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VQSLOD
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QD
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MQRankSum
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FS
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DP
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ClippingRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

East Asian
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allele 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

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 (Non-Finnish)
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allele count: 1
allele frequency: 1.541259517277519e-5
allele num: 64882
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

InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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QD
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ClippingRankSum
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MQ
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FS
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BaseQRankSum
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

European (Non-Finnish)
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allele count: 1
allele frequency: 1.542353013757789e-5
allele num: 64836
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6228
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8538
num of homozygotes: 0

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
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

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

DP
type: SiteQuality
SIO_000300: 1.566869e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

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

FS
type: SiteQuality
SIO_000300: 3.523e0

VQSLOD
type: SiteQuality
SIO_000300: -4.34e-1

MQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.09e-1

BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
allele num: 16272
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6212
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.841732979664014e-5
allele num: 11310
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.090043878623076e-5
allele num: 64724
num of homozygotes: 0

ClippingRankSum
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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DP
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FS
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6.150061500615006e-5
allele num: 16260
num of homozygotes: 0

East Asian
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allele frequency: 1.173708920187793e-4
allele num: 8520
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.611863313990974e-4
allele num: 6204
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 11294
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.091859134897814e-5
allele num: 64686
num of homozygotes: 0

FS
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BaseQRankSum
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QD
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DP
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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African
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Latino
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FS
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InbreedingCoeff
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ClippingRankSum
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DP
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VQSLOD
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QD
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BaseQRankSum
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MQRankSum
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MQ
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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
all individuals: 149
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Latino
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allele frequency: 2.660046107465862e-4
allele num: 11278
num of homozygotes: 0

South Asian
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East Asian
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Other
type: Population
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African
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allele count: 0
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allele num: 10004
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64476
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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FS
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SIO_000300: 6.231e0

DP
type: SiteQuality
SIO_000300: 1.550341e6

ClippingRankSum
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SIO_000300: 2.86e-1

MQ
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SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.43e-1

MQRankSum
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SIO_000300: 2.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

QD
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SIO_000300: 1.12e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.162455330318459e-5
allele num: 63242
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5990
num of homozygotes: 0

QD
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InbreedingCoeff
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DP
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: -5.73e-1

MQ
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SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.98e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.19e0

MQRankSum
type: SiteQuality
SIO_000300: 1.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5968
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11028
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.203369434416366e-4
allele num: 8310
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 count: 0
allele frequency: 0.0e0
allele num: 9722
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

FS
type: SiteQuality
SIO_000300: 6.196e0

InbreedingCoeff
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SIO_000300: 1.7e-3

MQ
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SIO_000300: 5.866e1

ClippingRankSum
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SIO_000300: 1.27e-1

DP
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SIO_000300: 1.493952e6

BaseQRankSum
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SIO_000300: -1.971e0

QD
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SIO_000300: 9.31e0

VQSLOD
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SIO_000300: -1.541e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.2e-2

GenotypeQuality
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variant carriers: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

East Asian
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allele count: 3
allele frequency: 3.610108303249097e-4
allele num: 8310
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63060
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9722
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11028
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5968
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16002
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.0e-2

FS
type: SiteQuality
SIO_000300: 6.196e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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SIO_000300: 1.27e-1

QD
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VQSLOD
type: SiteQuality
SIO_000300: -1.541e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.971e0

DP
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SIO_000300: 1.493952e6

MQ
type: SiteQuality
SIO_000300: 5.866e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 15948
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10972
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9656
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.779505480499618e-5
allele num: 62768
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8256
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5926
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.27e-1

ReadPosRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 9.31e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

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

Other
type: Population
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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
allele num: 15874
num of homozygotes: 0

Latino
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allele frequency: 2.755326965466569e-4
allele num: 10888
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 (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62498
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5902
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DP
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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FS
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QD
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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MQ
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SIO_000300: 5.907e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
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num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15844
num of homozygotes: 0

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

Other
type: Population
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 14
allele frequency: 2.244956864757384e-4
allele num: 62362
num of homozygotes: 0

Latino
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allele frequency: 2.855037760176828e-3
allele num: 10858
num of homozygotes: 1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5570
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 4
allele frequency: 6.695905453814992e-5
allele num: 59738
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.1e-2

QD
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FS
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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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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1240
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12646
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1496
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 959
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29636
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2274
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1039
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5322
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.699350847976073e-5
allele num: 58846
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8990
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7720
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9974
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 5.2e-1

FS
type: SiteQuality
SIO_000300: 1.139e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.86e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.294e0

MQRankSum
type: SiteQuality
SIO_000300: 3.51e-1

DP
type: SiteQuality
SIO_000300: 1.307055e6

VQSLOD
type: SiteQuality
SIO_000300: -5.846e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.471e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

GenotypeQuality
all individuals: 1024
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2389
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1623
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5222
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1218
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58358
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9808
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5400
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.259445843828715e-3
allele num: 794
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8928
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15188
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.283132e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.999999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.745e0

MQRankSum
type: SiteQuality
SIO_000300: -9.7e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.173e1

FS
type: SiteQuality
SIO_000300: 4.297e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

GenotypeQuality
all individuals: 933
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1800
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 638
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 941
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 14777
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1143
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26481
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 768
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2790
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2605
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4909
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9484
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 5.349023803155924e-4
allele num: 7478
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8750
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15028
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57306
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 778
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.554e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.177e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

FS
type: SiteQuality
SIO_000300: 2.278e0

QD
type: SiteQuality
SIO_000300: 9.289999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.359e0

MQRankSum
type: SiteQuality
SIO_000300: -2.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e0

DP
type: SiteQuality
SIO_000300: 1.241302e6

GenotypeQuality
all individuals: 778
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2679
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 5.75e1
variant carriers: 0