3-189584451-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584451
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584451
    reference: chr 3
allele count: 1
allele frequency: 9.0046283789868e-6
allele num: 111054
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.512-20T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.767-20T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.485-20T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.767-20T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.767-20T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.591-20T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.485-20T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.485-20T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.485-20T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.767-20T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.767-20T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.485-20T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.230-20T>C
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5739
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2442
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

3-189584461-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584461
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584461
    reference: chr 3
allele count: 1
allele frequency: 8.452799567216662e-6
allele num: 118304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.485-10T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.591-10T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.485-10T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.485-10T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.512-10T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.767-10T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.485-10T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.230-10T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.767-10T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.485-10T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.767-10T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.767-10T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.767-10T>C
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-189584487-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584487
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584487
    reference: chr 3
allele count: 4
allele frequency: 3.301746623964077e-5
allele num: 121148
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.607T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.501T>C
  hgvsp: ENST00000354600.5:c.501T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.783T>C
  hgvsp: ENST00000320472.5:c.783T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.783T>C
  hgvsp: ENST00000392460.3:c.783T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.783T>C
  hgvsp: ENST00000440651.2:c.783T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.501T>C
  hgvsp: ENST00000392463.2:c.501T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.501T>C
  hgvsp: ENST00000456148.1:c.501T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.501T>C
  hgvsp: ENST00000437221.1:c.501T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.501T>C
  hgvsp: ENST00000392461.3:c.501T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.783T>C
  hgvsp: ENST00000264731.3:c.783T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.246T>C
  hgvsp: ENST00000449992.1:c.246T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.783T>C
  hgvsp: ENST00000418709.2:c.783T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.528T>C
  hgvsp: ENST00000382063.4:c.528T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro261Pro
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: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/3-189584500-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584500
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584500
    reference: chr 3
allele count: 1
allele frequency: 8.24783082049421e-6
allele num: 121244
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.796C>A
  hgvsp: ENST00000392460.3:c.796C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.514C>A
  hgvsp: ENST00000392463.2:c.514C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.514C>A
  hgvsp: ENST00000437221.1:c.514C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.541C>A
  hgvsp: ENST00000382063.4:c.541C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.514C>A
  hgvsp: ENST00000354600.5:c.514C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.796C>A
  hgvsp: ENST00000440651.2:c.796C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.796C>A
  hgvsp: ENST00000264731.3:c.796C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.796C>A
  hgvsp: ENST00000320472.5:c.796C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.514C>A
  hgvsp: ENST00000392461.3:c.514C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.259C>A
  hgvsp: ENST00000449992.1:c.259C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.620C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.514C>A
  hgvsp: ENST00000456148.1:c.514C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.796C>A
  hgvsp: ENST00000418709.2:c.796C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg266Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

3-189584503-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584503
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584503
    reference: chr 3
allele count: 2
allele frequency: 1.649022129876983e-5
allele num: 121284
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.799G>A
  hgvsp: ENSP00000317510.5:p.Val267Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.799G>A
  hgvsp: ENSP00000407144.2:p.Val267Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.517G>A
  hgvsp: ENSP00000376254.3:p.Val173Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.544G>A
  hgvsp: ENSP00000371495.3:p.Val182Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.799G>A
  hgvsp: ENSP00000264731.3:p.Val267Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.517G>A
  hgvsp: ENSP00000392488.1:p.Val173Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.799G>A
  hgvsp: ENSP00000376253.3:p.Val267Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.517G>A
  hgvsp: ENSP00000346614.5:p.Val173Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.262G>A
  hgvsp: ENSP00000387839.1:p.Val88Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.517G>A
  hgvsp: ENSP00000376256.2:p.Val173Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.517G>A
  hgvsp: ENSP00000389485.1:p.Val173Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.623G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.799G>A
  hgvsp: ENSP00000394337.2:p.Val267Ile
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val267Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

3-189584503-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584503
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584503
    reference: chr 3
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.799G>T
  hgvsp: ENSP00000394337.2:p.Val267Leu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.262G>T
  hgvsp: ENSP00000387839.1:p.Val88Leu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.799G>T
  hgvsp: ENSP00000264731.3:p.Val267Leu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.799G>T
  hgvsp: ENSP00000407144.2:p.Val267Leu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.517G>T
  hgvsp: ENSP00000376254.3:p.Val173Leu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.799G>T
  hgvsp: ENSP00000317510.5:p.Val267Leu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.623G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.517G>T
  hgvsp: ENSP00000376256.2:p.Val173Leu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.517G>T
  hgvsp: ENSP00000346614.5:p.Val173Leu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.799G>T
  hgvsp: ENSP00000376253.3:p.Val267Leu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.517G>T
  hgvsp: ENSP00000389485.1:p.Val173Leu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.544G>T
  hgvsp: ENSP00000371495.3:p.Val182Leu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.517G>T
  hgvsp: ENSP00000392488.1:p.Val173Leu
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val267Leu
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

3-189584511-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584511
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584511
    reference: chr 3
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.807G>T
  hgvsp: ENST00000440651.2:c.807G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.525G>T
  hgvsp: ENST00000456148.1:c.525G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.525G>T
  hgvsp: ENST00000392463.2:c.525G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.807G>T
  hgvsp: ENST00000418709.2:c.807G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.525G>T
  hgvsp: ENST00000437221.1:c.525G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.807G>T
  hgvsp: ENST00000320472.5:c.807G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.270G>T
  hgvsp: ENST00000449992.1:c.270G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.525G>T
  hgvsp: ENST00000354600.5:c.525G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.525G>T
  hgvsp: ENST00000392461.3:c.525G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.807G>T
  hgvsp: ENST00000264731.3:c.807G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.552G>T
  hgvsp: ENST00000382063.4:c.552G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.807G>T
  hgvsp: ENST00000392460.3:c.807G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.631G>T
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40869
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly269Gly
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

3-189584513-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584513
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584513
    reference: chr 3
allele count: 1
allele frequency: 8.242935804015958e-6
allele num: 121316
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.633A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.809A>G
  hgvsp: ENSP00000407144.2:p.Asn270Ser
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.527A>G
  hgvsp: ENSP00000389485.1:p.Asn176Ser
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.809A>G
  hgvsp: ENSP00000394337.2:p.Asn270Ser
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.809A>G
  hgvsp: ENSP00000317510.5:p.Asn270Ser
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.554A>G
  hgvsp: ENSP00000371495.3:p.Asn185Ser
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.527A>G
  hgvsp: ENSP00000376254.3:p.Asn176Ser
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.527A>G
  hgvsp: ENSP00000346614.5:p.Asn176Ser
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.527A>G
  hgvsp: ENSP00000376256.2:p.Asn176Ser
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.809A>G
  hgvsp: ENSP00000264731.3:p.Asn270Ser
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.527A>G
  hgvsp: ENSP00000392488.1:p.Asn176Ser
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.809A>G
  hgvsp: ENSP00000376253.3:p.Asn270Ser
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.272A>G
  hgvsp: ENSP00000387839.1:p.Asn91Ser
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn270Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

3-189584529-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584529
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584529
    reference: chr 3
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.570T>C
  hgvsp: ENST00000382063.4:c.570T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.825T>C
  hgvsp: ENST00000320472.5:c.825T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.543T>C
  hgvsp: ENST00000456148.1:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.543T>C
  hgvsp: ENST00000354600.5:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.825T>C
  hgvsp: ENST00000392460.3:c.825T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.825T>C
  hgvsp: ENST00000440651.2:c.825T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.543T>C
  hgvsp: ENST00000437221.1:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.543T>C
  hgvsp: ENST00000392461.3:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.543T>C
  hgvsp: ENST00000392463.2:c.543T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.288T>C
  hgvsp: ENST00000449992.1:c.288T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.825T>C
  hgvsp: ENST00000264731.3:c.825T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.825T>C
  hgvsp: ENST00000418709.2:c.825T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.649T>C
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8430
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr275Tyr
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS

3-189584538-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584538
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584538
    reference: chr 3
allele count: 1
allele frequency: 8.240762105679534e-6
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.552T>C
  hgvsp: ENST00000437221.1:c.552T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.834T>C
  hgvsp: ENST00000418709.2:c.834T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.834T>C
  hgvsp: ENST00000440651.2:c.834T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.579T>C
  hgvsp: ENST00000382063.4:c.579T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.834T>C
  hgvsp: ENST00000392460.3:c.834T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.552T>C
  hgvsp: ENST00000354600.5:c.552T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.834T>C
  hgvsp: ENST00000320472.5:c.834T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.552T>C
  hgvsp: ENST00000456148.1:c.552T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.834T>C
  hgvsp: ENST00000264731.3:c.834T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.552T>C
  hgvsp: ENST00000392463.2:c.552T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.552T>C
  hgvsp: ENST00000392461.3:c.552T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.658T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.297T>C
  hgvsp: ENST00000449992.1:c.297T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp278Asp
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum

3-189584543-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584543
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584543
    reference: chr 3
allele count: 149
allele frequency: 1.227893791307501e-3
allele num: 121346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.839T>A
  hgvsp: ENSP00000394337.2:p.Ile280Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.557T>A
  hgvsp: ENSP00000346614.5:p.Ile186Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.839T>A
  hgvsp: ENSP00000407144.2:p.Ile280Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.584T>A
  hgvsp: ENSP00000371495.3:p.Ile195Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.839T>A
  hgvsp: ENSP00000264731.3:p.Ile280Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.839T>A
  hgvsp: ENSP00000317510.5:p.Ile280Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.557T>A
  hgvsp: ENSP00000389485.1:p.Ile186Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.557T>A
  hgvsp: ENSP00000392488.1:p.Ile186Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.557T>A
  hgvsp: ENSP00000376254.3:p.Ile186Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.557T>A
  hgvsp: ENSP00000376256.2:p.Ile186Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.663T>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.839T>A
  hgvsp: ENSP00000376253.3:p.Ile280Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.302T>A
  hgvsp: ENSP00000387839.1:p.Ile101Asn
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 8421
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 9.75e1
  variant carriers: 67
genotype quality: GenotypeQuality
hgvs: p.Ile280Asn
num of homozygotes: 1
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

3-189584554-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584554
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584554
    reference: chr 3
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.850C>G
  hgvsp: ENSP00000317510.5:p.Gln284Glu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.568C>G
  hgvsp: ENSP00000376256.2:p.Gln190Glu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.674C>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.568C>G
  hgvsp: ENSP00000346614.5:p.Gln190Glu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.595C>G
  hgvsp: ENSP00000371495.3:p.Gln199Glu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.568C>G
  hgvsp: ENSP00000376254.3:p.Gln190Glu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.850C>G
  hgvsp: ENSP00000264731.3:p.Gln284Glu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.568C>G
  hgvsp: ENSP00000389485.1:p.Gln190Glu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.313C>G
  hgvsp: ENSP00000387839.1:p.Gln105Glu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.850C>G
  hgvsp: ENSP00000407144.2:p.Gln284Glu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.850C>G
  hgvsp: ENSP00000394337.2:p.Gln284Glu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.850C>G
  hgvsp: ENSP00000376253.3:p.Gln284Glu
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.568C>G
  hgvsp: ENSP00000392488.1:p.Gln190Glu
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40671
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1100
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8489
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln284Glu
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

3-189584558-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584558
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584558
    reference: chr 3
allele count: 2
allele frequency: 1.64836976230508e-5
allele num: 121332
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.572G>A
  hgvsp: ENSP00000392488.1:p.Ser191Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.599G>A
  hgvsp: ENSP00000371495.3:p.Ser200Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.678G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.572G>A
  hgvsp: ENSP00000376256.2:p.Ser191Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.854G>A
  hgvsp: ENSP00000376253.3:p.Ser285Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.572G>A
  hgvsp: ENSP00000376254.3:p.Ser191Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.317G>A
  hgvsp: ENSP00000387839.1:p.Ser106Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.854G>A
  hgvsp: ENSP00000394337.2:p.Ser285Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.572G>A
  hgvsp: ENSP00000346614.5:p.Ser191Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.854G>A
  hgvsp: ENSP00000317510.5:p.Ser285Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.572G>A
  hgvsp: ENSP00000389485.1:p.Ser191Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.854G>A
  hgvsp: ENSP00000264731.3:p.Ser285Asn
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.854G>A
  hgvsp: ENSP00000407144.2:p.Ser285Asn
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser285Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

3-189584562-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584562
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584562
    reference: chr 3
allele count: 1
allele frequency: 8.242120532770671e-6
allele num: 121328
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.603G>T
  hgvsp: ENST00000382063.4:c.603G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.576G>T
  hgvsp: ENST00000437221.1:c.576G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.858G>T
  hgvsp: ENST00000264731.3:c.858G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.576G>T
  hgvsp: ENST00000456148.1:c.576G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.858G>T
  hgvsp: ENST00000320472.5:c.858G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.321G>T
  hgvsp: ENST00000449992.1:c.321G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.858G>T
  hgvsp: ENST00000392460.3:c.858G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.576G>T
  hgvsp: ENST00000392463.2:c.576G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.576G>T
  hgvsp: ENST00000354600.5:c.576G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.858G>T
  hgvsp: ENST00000418709.2:c.858G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.858G>T
  hgvsp: ENST00000440651.2:c.858G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.682G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.576G>T
  hgvsp: ENST00000392461.3:c.576G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40613
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8485
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val286Val
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

3-189584563-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584563
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584563
    reference: chr 3
allele count: 2006
allele frequency: 1.653423889749761e-2
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.859C>T
  hgvsp: ENST00000418709.2:c.859C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.577C>T
  hgvsp: ENST00000354600.5:c.577C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.859C>T
  hgvsp: ENST00000440651.2:c.859C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.859C>T
  hgvsp: ENST00000392460.3:c.859C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.577C>T
  hgvsp: ENST00000392461.3:c.577C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.577C>T
  hgvsp: ENST00000437221.1:c.577C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.322C>T
  hgvsp: ENST00000449992.1:c.322C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.577C>T
  hgvsp: ENST00000456148.1:c.577C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.577C>T
  hgvsp: ENST00000392463.2:c.577C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.604C>T
  hgvsp: ENST00000382063.4:c.604C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.859C>T
  hgvsp: ENST00000320472.5:c.859C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.859C>T
  hgvsp: ENST00000264731.3:c.859C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.683C>T
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 6.25e1
  variant carriers: 158
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 5.25e1
  variant carriers: 134
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 6.75e1
  variant carriers: 148
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 82
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 7.75e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 4.25e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 876
  bin: 3.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 8268
  bin: 2.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39343
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 8.25e1
  variant carriers: 105
genotype quality: GenotypeQuality
hgvs: p.Leu287Leu
num of homozygotes: 27
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
reference allele: C
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

3-189584565-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584565
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584565
    reference: chr 3
allele count: 3
allele frequency: 2.472962279082036e-5
allele num: 121312
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.861G>A
  hgvsp: ENST00000320472.5:c.861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.861G>A
  hgvsp: ENST00000392460.3:c.861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.579G>A
  hgvsp: ENST00000392463.2:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.579G>A
  hgvsp: ENST00000354600.5:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.861G>A
  hgvsp: ENST00000264731.3:c.861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.579G>A
  hgvsp: ENST00000392461.3:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.579G>A
  hgvsp: ENST00000437221.1:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.685G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.324G>A
  hgvsp: ENST00000449992.1:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.861G>A
  hgvsp: ENST00000418709.2:c.861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.606G>A
  hgvsp: ENST00000382063.4:c.606G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.861G>A
  hgvsp: ENST00000440651.2:c.861G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.579G>A
  hgvsp: ENST00000456148.1:c.579G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu287Leu
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

3-189584577-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584577
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584577
    reference: chr 3
allele count: 2
allele frequency: 1.650355651642929e-5
allele num: 121186
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.591G>A
  hgvsp: ENST00000392463.2:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.591G>A
  hgvsp: ENST00000437221.1:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.336G>A
  hgvsp: ENST00000449992.1:c.336G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.591G>A
  hgvsp: ENST00000392461.3:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.591G>A
  hgvsp: ENST00000456148.1:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.873G>A
  hgvsp: ENST00000418709.2:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.873G>A
  hgvsp: ENST00000264731.3:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.873G>A
  hgvsp: ENST00000392460.3:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.591G>A
  hgvsp: ENST00000354600.5:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.618G>A
  hgvsp: ENST00000382063.4:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.697G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.873G>A
  hgvsp: ENST00000440651.2:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.873G>A
  hgvsp: ENST00000320472.5:c.873G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu291Glu
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/3-189584578-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584578
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584578
    reference: chr 3
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.619C>A
  hgvsp: ENSP00000371495.3:p.Pro207Thr
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.592C>A
  hgvsp: ENSP00000389485.1:p.Pro198Thr
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.592C>A
  hgvsp: ENSP00000376256.2:p.Pro198Thr
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.592C>A
  hgvsp: ENSP00000346614.5:p.Pro198Thr
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.337C>A
  hgvsp: ENSP00000387839.1:p.Pro113Thr
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.874C>A
  hgvsp: ENSP00000317510.5:p.Pro292Thr
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.874C>A
  hgvsp: ENSP00000264731.3:p.Pro292Thr
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.592C>A
  hgvsp: ENSP00000376254.3:p.Pro198Thr
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.874C>A
  hgvsp: ENSP00000376253.3:p.Pro292Thr
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.874C>A
  hgvsp: ENSP00000394337.2:p.Pro292Thr
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.592C>A
  hgvsp: ENSP00000392488.1:p.Pro198Thr
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.874C>A
  hgvsp: ENSP00000407144.2:p.Pro292Thr
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.698C>A
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9114
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro292Thr
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

3-189584578-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584578
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584578
    reference: chr 3
allele count: 2
allele frequency: 1.650246711883427e-5
allele num: 121194
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.592C>G
  hgvsp: ENSP00000346614.5:p.Pro198Ala
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.874C>G
  hgvsp: ENSP00000394337.2:p.Pro292Ala
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.698C>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.592C>G
  hgvsp: ENSP00000389485.1:p.Pro198Ala
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.874C>G
  hgvsp: ENSP00000407144.2:p.Pro292Ala
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.874C>G
  hgvsp: ENSP00000317510.5:p.Pro292Ala
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.874C>G
  hgvsp: ENSP00000264731.3:p.Pro292Ala
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.874C>G
  hgvsp: ENSP00000376253.3:p.Pro292Ala
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.592C>G
  hgvsp: ENSP00000392488.1:p.Pro198Ala
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.592C>G
  hgvsp: ENSP00000376256.2:p.Pro198Ala
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.592C>G
  hgvsp: ENSP00000376254.3:p.Pro198Ala
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.619C>G
  hgvsp: ENSP00000371495.3:p.Pro207Ala
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.337C>G
  hgvsp: ENSP00000387839.1:p.Pro113Ala
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro292Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

3-189584588-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584588
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584588
    reference: chr 3
allele count: 1
allele frequency: 8.278831029058698e-6
allele num: 120790
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.600+2T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.882+2T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.882+2T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.600+2T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.706+2T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.882+2T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.600+2T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.882+2T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.600+2T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.345+2T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.600+2T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.627+2T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.882+2T>G
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: splice donor
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8997
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38307
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.882+2T>G
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

3-189584594-GCAAAAAACCAAAC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584594
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584581
    reference: chr 3
allele count: 1
allele frequency: 8.307027745472669e-6
allele num: 120380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: GCAAAAAACCAAAC
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

3-189584594-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584594
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584594
    reference: chr 3
allele count: 1
allele frequency: 8.307027745472669e-6
allele num: 120380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.600+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.627+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.600+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.345+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.882+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.882+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.882+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.600+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.882+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.600+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.706+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.600+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.882+8G>A
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.882+8G>A
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

3-189584596-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584596
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584596
    reference: chr 3
allele count: 1
allele frequency: 8.325285557294615e-6
allele num: 120116
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.706+10A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.600+10A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.882+10A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.600+10A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.600+10A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.882+10A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.600+10A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.882+10A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.882+10A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.882+10A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.627+10A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.600+10A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.345+10A>G
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 865
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/3-189584602-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584602
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584602
    reference: chr 3
allele count: 31
allele frequency: 2.591799879606715e-4
allele num: 119608
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.882+16C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.882+16C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.706+16C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.600+16C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.627+16C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.600+16C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.345+16C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.882+16C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.600+16C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.882+16C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.600+16C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.882+16C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.600+16C>A
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34078
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8672
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3844
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

3-189584604-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584604
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584604
    reference: chr 3
allele count: 17
allele frequency: 1.424883494820129e-4
allele num: 119308
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.600+18A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.882+18A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.345+18A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.627+18A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.600+18A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.882+18A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.600+18A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.600+18A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.706+18A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.882+18A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.600+18A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.882+18A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.882+18A>G
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8268
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31848
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

3-189584604-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584604
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584604
    reference: chr 3
allele count: 1
allele frequency: 8.381667616588997e-6
allele num: 119308
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.345+18A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.627+18A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.600+18A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.600+18A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.600+18A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.882+18A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.882+18A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.882+18A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.706+18A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.882+18A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.600+18A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.882+18A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.600+18A>T
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31848
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 955
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2668
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum

3-189584605-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584605
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584605
    reference: chr 3
allele count: 1
allele frequency: 8.386447500838645e-6
allele num: 119240
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.882+19A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.600+19A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.882+19A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.882+19A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.600+19A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.600+19A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.882+19A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.706+19A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.600+19A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.882+19A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.600+19A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.627+19A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.345+19A>G
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

3-189584605-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584605
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584605
    reference: chr 3
allele count: 2
allele frequency: 1.677289500167729e-5
allele num: 119240
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.882+19A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.882+19A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.600+19A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.345+19A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.706+19A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.882+19A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.600+19A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.882+19A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.600+19A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.600+19A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.882+19A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.600+19A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.627+19A>T
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8311
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/3-189584606-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584606
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584606
    reference: chr 3
allele count: 1
allele frequency: 8.393627557957998e-6
allele num: 119138
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.706+20A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.345+20A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.600+20A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.627+20A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.882+20A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.882+20A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.882+20A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.882+20A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.600+20A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.882+20A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.600+20A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.600+20A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.600+20A>C
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5953
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/3-189584608-CAAAAAA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584608
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584602
    reference: chr 3
allele count: 5
allele frequency: 4.213577833209735e-5
allele num: 118664
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.882+23_882+28delAAAAAA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.627+23_627+28delAAAAAA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.600+23_600+28delAAAAAA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.882+23_882+28delAAAAAA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.882+23_882+28delAAAAAA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.600+23_600+28delAAAAAA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.600+23_600+28delAAAAAA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.882+23_882+28delAAAAAA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.706+23_706+28delAAAAAA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.345+23_345+28delAAAAAA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.882+23_882+28delAAAAAA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.600+23_600+28delAAAAAA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.600+23_600+28delAAAAAA
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28691
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: CAAAAAA
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

3-189584611-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584611
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584611
    reference: chr 3
allele count: 1
allele frequency: 8.419634587858886e-6
allele num: 118770
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.706+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.600+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.627+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.882+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.600+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.882+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.345+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.600+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.882+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.882+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.600+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.882+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.600+25A>G
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7750
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

3-189584626-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584626
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584626
    reference: chr 3
allele count: 2
allele frequency: 1.718331156780535e-5
allele num: 116392
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.882+40T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.882+40T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.882+40T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.882+40T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.600+40T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.600+40T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.627+40T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.600+40T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.600+40T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.600+40T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.345+40T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.882+40T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.706+40T>C
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 856
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10280
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17780
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

3-189584631-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584631
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584631
    reference: chr 3
allele count: 1
allele frequency: 8.753961167428261e-6
allele num: 114234
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.600+45T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.345+45T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.600+45T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.882+45T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.600+45T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.600+45T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.882+45T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.882+45T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.706+45T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.627+45T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.600+45T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.882+45T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.882+45T>G
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17506
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9919
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP

3-189584634-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189584634
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189584634
    reference: chr 3
allele count: 1
allele frequency: 8.746610688358261e-6
allele num: 114330
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.882+48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.627+48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.600+48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.706+48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.882+48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.600+48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.600+48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.600+48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.882+48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.600+48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.882+48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.345+48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.882+48G>A
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9966
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1705
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17447
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

3-189585573-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585573
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585573
    reference: chr 3
allele count: 2
allele frequency: 1.865428022459753e-5
allele num: 107214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.883-49C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.601-49C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.707-49C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.346-49C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.883-49C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.628-49C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.601-49C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.883-49C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.601-49C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.601-49C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.601-49C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.883-49C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.883-49C>T
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6259
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16720
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8797
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3726
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

3-189585574-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585574
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585574
    reference: chr 3
allele count: 6
allele frequency: 5.596492864471598e-5
allele num: 107210
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.883-48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.883-48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.601-48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.883-48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.601-48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.601-48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.707-48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.601-48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.346-48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.601-48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.883-48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.883-48G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.628-48G>A
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9705
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16693
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6242
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3748
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1247
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

3-189585579-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585579
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585579
    reference: chr 3
allele count: 2
allele frequency: 1.851029172219754e-5
allele num: 108048
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.601-43T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.883-43T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.628-43T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.346-43T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.707-43T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.883-43T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.601-43T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.601-43T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.601-43T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.883-43T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.883-43T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.883-43T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.601-43T>C
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9587
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14208
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/3-189585585-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585585
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585585
    reference: chr 3
allele count: 1
allele frequency: 9.229349330872173e-6
allele num: 108350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.883-37C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.601-37C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.883-37C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.707-37C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.601-37C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.601-37C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.601-37C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.883-37C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.883-37C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.628-37C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.883-37C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.601-37C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.346-37C>A
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6059
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5830
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD

3-189585585-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585585
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585585
    reference: chr 3
allele count: 1
allele frequency: 9.229349330872173e-6
allele num: 108350
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.883-37C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.707-37C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.601-37C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.601-37C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.601-37C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.628-37C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.883-37C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.601-37C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.883-37C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.346-37C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.601-37C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.883-37C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.883-37C>T
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5830
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6059
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

3-189585587-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585587
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585587
    reference: chr 3
allele count: 1
allele frequency: 9.20030913038678e-6
allele num: 108692
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.883-35C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.601-35C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.346-35C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.601-35C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.601-35C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.707-35C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.883-35C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.601-35C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.601-35C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.883-35C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.883-35C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.628-35C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.883-35C>T
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21832
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5893
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12833
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

3-189585590-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585590
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585590
    reference: chr 3
allele count: 2
allele frequency: 1.827652380517226e-5
allele num: 109430
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.601-32G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.707-32G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.601-32G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.883-32G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.601-32G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.601-32G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.601-32G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.628-32G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.883-32G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.883-32G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.883-32G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.883-32G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.346-32G>T
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11030
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5661
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5159
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

3-189585597-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585597
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585597
    reference: chr 3
allele count: 1
allele frequency: 8.952711776397071e-6
allele num: 111698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.601-25C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.883-25C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.346-25C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.601-25C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.601-25C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.883-25C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.707-25C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.601-25C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.601-25C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.628-25C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.883-25C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.883-25C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.883-25C>T
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6122
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

3-189585598-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585598
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585598
    reference: chr 3
allele count: 7
allele frequency: 6.241195456409707e-5
allele num: 112158
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.601-24A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.601-24A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.628-24A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.883-24A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.601-24A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.883-24A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.601-24A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.707-24A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.883-24A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.883-24A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.601-24A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.346-24A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.883-24A>G
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5925
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6226
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

3-189585613-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585613
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585613
    reference: chr 3
allele count: 1
allele frequency: 8.539563799081142e-6
allele num: 117102
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.601-9T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.601-9T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.883-9T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.601-9T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.883-9T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.601-9T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.883-9T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.707-9T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.628-9T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.601-9T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.346-9T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.883-9T>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.883-9T>G
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1616
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

3-189585627-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585627
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585627
    reference: chr 3
allele count: 1
allele frequency: 8.337780149413021e-6
allele num: 119936
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.606C>G
  hgvsp: ENST00000392461.3:c.606C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.712C>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.888C>G
  hgvsp: ENST00000440651.2:c.888C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.351C>G
  hgvsp: ENST00000449992.1:c.351C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.888C>G
  hgvsp: ENST00000320472.5:c.888C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.606C>G
  hgvsp: ENST00000354600.5:c.606C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.606C>G
  hgvsp: ENST00000456148.1:c.606C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.888C>G
  hgvsp: ENST00000264731.3:c.888C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.606C>G
  hgvsp: ENST00000392463.2:c.606C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.888C>G
  hgvsp: ENST00000392460.3:c.888C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.888C>G
  hgvsp: ENST00000418709.2:c.888C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.606C>G
  hgvsp: ENST00000437221.1:c.606C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.633C>G
  hgvsp: ENST00000382063.4:c.633C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly296Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

3-189585630-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585630
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585630
    reference: chr 3
allele count: 2
allele frequency: 1.664031949413429e-5
allele num: 120190
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.891T>A
  hgvsp: ENST00000392460.3:c.891T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.609T>A
  hgvsp: ENST00000392463.2:c.609T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.609T>A
  hgvsp: ENST00000354600.5:c.609T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.891T>A
  hgvsp: ENST00000440651.2:c.891T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.891T>A
  hgvsp: ENST00000264731.3:c.891T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.891T>A
  hgvsp: ENST00000418709.2:c.891T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.609T>A
  hgvsp: ENST00000392461.3:c.609T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.636T>A
  hgvsp: ENST00000382063.4:c.636T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.609T>A
  hgvsp: ENST00000456148.1:c.609T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.715T>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.891T>A
  hgvsp: ENST00000320472.5:c.891T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.354T>A
  hgvsp: ENST00000449992.1:c.354T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.609T>A
  hgvsp: ENST00000437221.1:c.609T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9098
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr297Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

3-189585639-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585639
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585639
    reference: chr 3
allele count: 7
allele frequency: 5.805274506551667e-5
allele num: 120580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.900G>A
  hgvsp: ENST00000320472.5:c.900G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.724G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.900G>A
  hgvsp: ENST00000264731.3:c.900G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.618G>A
  hgvsp: ENST00000354600.5:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.363G>A
  hgvsp: ENST00000449992.1:c.363G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.618G>A
  hgvsp: ENST00000437221.1:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.900G>A
  hgvsp: ENST00000440651.2:c.900G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.618G>A
  hgvsp: ENST00000392461.3:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.900G>A
  hgvsp: ENST00000392460.3:c.900G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.618G>A
  hgvsp: ENST00000456148.1:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.618G>A
  hgvsp: ENST00000392463.2:c.618G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.645G>A
  hgvsp: ENST00000382063.4:c.645G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.900G>A
  hgvsp: ENST00000418709.2:c.900G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr300Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

3-189585657-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585657
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585657
    reference: chr 3
allele count: 1
allele frequency: 8.278968109414843e-6
allele num: 120788
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.636C>T
  hgvsp: ENST00000392461.3:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.918C>T
  hgvsp: ENST00000392460.3:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.636C>T
  hgvsp: ENST00000354600.5:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.636C>T
  hgvsp: ENST00000392463.2:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.918C>T
  hgvsp: ENST00000440651.2:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.636C>T
  hgvsp: ENST00000437221.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.918C>T
  hgvsp: ENST00000418709.2:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.918C>T
  hgvsp: ENST00000320472.5:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.663C>T
  hgvsp: ENST00000382063.4:c.663C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.636C>T
  hgvsp: ENST00000456148.1:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.381C>T
  hgvsp: ENST00000449992.1:c.381C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.742C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.918C>T
  hgvsp: ENST00000264731.3:c.918C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9643
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe306Phe
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

3-189585676-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585676
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585676
    reference: chr 3
allele count: 1
allele frequency: 8.287475966319697e-6
allele num: 120664
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.655G>A
  hgvsp: ENSP00000376254.3:p.Val219Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.655G>A
  hgvsp: ENSP00000392488.1:p.Val219Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.761G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.937G>A
  hgvsp: ENSP00000376253.3:p.Val313Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.655G>A
  hgvsp: ENSP00000346614.5:p.Val219Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.937G>A
  hgvsp: ENSP00000317510.5:p.Val313Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.682G>A
  hgvsp: ENSP00000371495.3:p.Val228Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.937G>A
  hgvsp: ENSP00000407144.2:p.Val313Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.655G>A
  hgvsp: ENSP00000376256.2:p.Val219Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.400G>A
  hgvsp: ENSP00000387839.1:p.Val134Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.937G>A
  hgvsp: ENSP00000394337.2:p.Val313Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.937G>A
  hgvsp: ENSP00000264731.3:p.Val313Ile
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.655G>A
  hgvsp: ENSP00000389485.1:p.Val219Ile
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val313Ile
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

3-189585684-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585684
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585684
    reference: chr 3
allele count: 2
allele frequency: 1.661819692563357e-5
allele num: 120350
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.663G>A
  hgvsp: ENST00000392461.3:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.945G>A
  hgvsp: ENST00000392460.3:c.945G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.663G>A
  hgvsp: ENST00000392463.2:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.945G>A
  hgvsp: ENST00000264731.3:c.945G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.663G>A
  hgvsp: ENST00000437221.1:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.663G>A
  hgvsp: ENST00000354600.5:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.663G>A
  hgvsp: ENST00000456148.1:c.663G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.408G>A
  hgvsp: ENST00000449992.1:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.945G>A
  hgvsp: ENST00000320472.5:c.945G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.769G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.945G>A
  hgvsp: ENST00000440651.2:c.945G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.945G>A
  hgvsp: ENST00000418709.2:c.945G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.690G>A
  hgvsp: ENST00000382063.4:c.690G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9909
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly315Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/3-189585693-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585693
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585693
    reference: chr 3
allele count: 2
allele frequency: 1.671709657466691e-5
allele num: 119638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.672C>A
  hgvsp: ENST00000456148.1:c.672C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.672C>A
  hgvsp: ENST00000392461.3:c.672C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.672C>A
  hgvsp: ENST00000354600.5:c.672C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.954C>A
  hgvsp: ENST00000264731.3:c.954C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.672C>A
  hgvsp: ENST00000392463.2:c.672C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.954C>A
  hgvsp: ENST00000392460.3:c.954C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.954C>A
  hgvsp: ENST00000320472.5:c.954C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.954C>A
  hgvsp: ENST00000440651.2:c.954C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.778C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.699C>A
  hgvsp: ENST00000382063.4:c.699C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.954C>A
  hgvsp: ENST00000418709.2:c.954C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.417C>A
  hgvsp: ENST00000449992.1:c.417C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.672C>A
  hgvsp: ENST00000437221.1:c.672C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9859
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38046
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg318Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum

3-189585696-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585696
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585696
    reference: chr 3
allele count: 4
allele frequency: 3.351768057650411e-5
allele num: 119340
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.957T>C
  hgvsp: ENST00000320472.5:c.957T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.675T>C
  hgvsp: ENST00000437221.1:c.675T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.675T>C
  hgvsp: ENST00000354600.5:c.675T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.420T>C
  hgvsp: ENST00000449992.1:c.420T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.957T>C
  hgvsp: ENST00000264731.3:c.957T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.675T>C
  hgvsp: ENST00000392461.3:c.675T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.675T>C
  hgvsp: ENST00000392463.2:c.675T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.781T>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.957T>C
  hgvsp: ENST00000392460.3:c.957T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.957T>C
  hgvsp: ENST00000418709.2:c.957T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.957T>C
  hgvsp: ENST00000440651.2:c.957T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.675T>C
  hgvsp: ENST00000456148.1:c.675T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.702T>C
  hgvsp: ENST00000382063.4:c.702T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37688
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg319Arg
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

3-189585718-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585718
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585718
    reference: chr 3
allele count: 1
allele frequency: 8.686738824510502e-6
allele num: 115118
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.697C>T
  hgvsp: ENST00000437221.1:c.697C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.979C>T
  hgvsp: ENST00000264731.3:c.979C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.979C>T
  hgvsp: ENST00000418709.2:c.979C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.697C>T
  hgvsp: ENST00000456148.1:c.697C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.979C>T
  hgvsp: ENST00000440651.2:c.979C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.442C>T
  hgvsp: ENST00000449992.1:c.442C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.697C>T
  hgvsp: ENST00000354600.5:c.697C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.979C>T
  hgvsp: ENST00000392460.3:c.979C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.724C>T
  hgvsp: ENST00000382063.4:c.724C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.697C>T
  hgvsp: ENST00000392461.3:c.697C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.697C>T
  hgvsp: ENST00000392463.2:c.697C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.803C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.979C>T
  hgvsp: ENST00000320472.5:c.979C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu327Leu
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

3-189585731-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585731
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585731
    reference: chr 3
allele count: 1
allele frequency: 9.202849202112974e-6
allele num: 108662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.710A>T
  hgvsp: ENSP00000392488.1:p.Asp237Val
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.737A>T
  hgvsp: ENSP00000371495.3:p.Asp246Val
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.455A>T
  hgvsp: ENSP00000387839.1:p.Asp152Val
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.710A>T
  hgvsp: ENSP00000376256.2:p.Asp237Val
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.710A>T
  hgvsp: ENSP00000346614.5:p.Asp237Val
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.992A>T
  hgvsp: ENSP00000394337.2:p.Asp331Val
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.816A>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.992A>T
  hgvsp: ENSP00000376253.3:p.Asp331Val
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.710A>T
  hgvsp: ENSP00000389485.1:p.Asp237Val
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.992A>T
  hgvsp: ENSP00000317510.5:p.Asp331Val
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.710A>T
  hgvsp: ENSP00000376254.3:p.Asp237Val
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.992A>T
  hgvsp: ENSP00000264731.3:p.Asp331Val
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.992A>T
  hgvsp: ENSP00000407144.2:p.Asp331Val
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1625
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp331Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/3-189585735-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585735
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585735
    reference: chr 3
allele count: 78
allele frequency: 7.334273624823696e-4
allele num: 106350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.992+4A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.710+4A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.710+4A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.737+4A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.992+4A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.992+4A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.992+4A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.710+4A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.455+4A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.710+4A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.816+4A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.992+4A>C
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.710+4A>C
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7281
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7099
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20497
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.992+4A>C
num of homozygotes: 2
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

3-189585739-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585739
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585739
    reference: chr 3
allele count: 5
allele frequency: 4.808802031237978e-5
allele num: 103976
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.737+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.455+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.710+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.710+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.816+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.710+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.710+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.992+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.710+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.992+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.992+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.992+8G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.992+8G>A
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6180
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8285
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15244
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.992+8G>A
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

3-189585740-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585740
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585740
    reference: chr 3
allele count: 1
allele frequency: 9.684667234833812e-6
allele num: 103256
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.710+9C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.992+9C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.710+9C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.992+9C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.992+9C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.816+9C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.455+9C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.710+9C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.710+9C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.992+9C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.710+9C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.737+9C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.992+9C>T
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15859
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8495
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

3-189585741-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585741
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585741
    reference: chr 3
allele count: 3
allele frequency: 2.925002925002925e-5
allele num: 102564
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.992+10G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.816+10G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.455+10G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.992+10G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.737+10G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.710+10G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.710+10G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.710+10G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.710+10G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.992+10G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.992+10G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.992+10G>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.710+10G>A
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8741
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3299
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16444
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-189585745-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585745
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585745
    reference: chr 3
allele count: 1
allele frequency: 9.909231440009513e-6
allele num: 100916
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.710+14G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.710+14G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.455+14G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.710+14G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.992+14G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.710+14G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.737+14G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.992+14G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.992+14G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.992+14G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.992+14G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.710+14G>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.816+14G>T
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9549
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18653
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

3-189585756-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585756
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585756
    reference: chr 3
allele count: 3
allele frequency: 3.094633904809061e-5
allele num: 96942
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.710+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.816+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.992+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.710+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.710+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.455+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.992+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.992+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.992+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.737+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.710+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.710+25A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.992+25A>G
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10932
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

3-189585764-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585764
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585764
    reference: chr 3
allele count: 2
allele frequency: 2.161601314253599e-5
allele num: 92524
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.992+33C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.710+33C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.992+33C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.816+33C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.710+33C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.455+33C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.737+33C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.710+33C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.992+33C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.992+33C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.710+33C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.992+33C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.710+33C>T
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11948
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23413
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/3-189585764-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585764
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585765
    reference: chr 3
allele count: 7
allele frequency: 7.565604599887597e-5
allele num: 92524
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.816+39dupA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.737+39dupA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.710+39dupA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.710+39dupA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.710+39dupA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.992+39dupA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.992+39dupA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.992+39dupA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.710+39dupA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.710+39dupA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.992+39dupA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.992+39dupA
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.455+39dupA
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1737
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23413
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11948
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7325
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum

3-189585770-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585770
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585770
    reference: chr 3
allele count: 2
allele frequency: 2.232192682872385e-5
allele num: 89598
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.992+39A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.455+39A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.992+39A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.710+39A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.992+39A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.992+39A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.816+39A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.710+39A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.737+39A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.710+39A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.992+39A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.710+39A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.710+39A>G
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2046
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8656
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

3-189585774-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585774
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585774
    reference: chr 3
allele count: 11
allele frequency: 1.276102088167053e-4
allele num: 86200
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.710+43C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.455+43C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.992+43C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.710+43C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.992+43C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.992+43C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.710+43C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.710+43C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.992+43C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.710+43C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.992+43C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.737+43C>T
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.816+43C>T
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8724
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14870
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21066
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/3-189585778-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189585778
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189585778
    reference: chr 3
allele count: 4
allele frequency: 4.781371775562409e-5
allele num: 83658
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.992+47C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.737+47C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.710+47C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.992+47C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.992+47C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.992+47C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.710+47C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.992+47C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.710+47C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.710+47C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.816+47C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.710+47C>A
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.455+47C>A
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1517
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8421
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20174
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16043
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

3-189586321-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 189586321
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 189586321
    reference: chr 3
allele count: 1
allele frequency: 8.652165637058956e-6
allele num: 115578
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000387839
  ensembl transcript: ENST00000449992
  gene symbol: TP63
  hgvsc: ENST00000449992.1:c.456-48A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl transcript: ENST00000460036
  gene symbol: TP63
  hgvsc: ENST00000460036.1:n.817-48A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000392488
  ensembl transcript: ENST00000437221
  gene symbol: TP63
  hgvsc: ENST00000437221.1:c.711-48A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000394337
  ensembl transcript: ENST00000440651
  gene symbol: TP63
  hgvsc: ENST00000440651.2:c.993-48A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376253
  ensembl transcript: ENST00000392460
  gene symbol: TP63
  hgvsc: ENST00000392460.3:c.993-48A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376256
  ensembl transcript: ENST00000392463
  gene symbol: TP63
  hgvsc: ENST00000392463.2:c.711-48A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000346614
  ensembl transcript: ENST00000354600
  gene symbol: TP63
  hgvsc: ENST00000354600.5:c.711-48A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000317510
  ensembl transcript: ENST00000320472
  gene symbol: TP63
  hgvsc: ENST00000320472.5:c.993-48A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000371495
  ensembl transcript: ENST00000382063
  gene symbol: TP63
  hgvsc: ENST00000382063.4:c.738-48A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000389485
  ensembl transcript: ENST00000456148
  gene symbol: TP63
  hgvsc: ENST00000456148.1:c.711-48A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000407144
  ensembl transcript: ENST00000418709
  gene symbol: TP63
  hgvsc: ENST00000418709.2:c.993-48A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000264731
  ensembl transcript: ENST00000264731
  gene symbol: TP63
  hgvsc: ENST00000264731.3:c.993-48A>G
  variant of: http://identifiers.org/hgnc/15979
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000073282
  ensembl protein: ENSP00000376254
  ensembl transcript: ENST00000392461
  gene symbol: TP63
  hgvsc: ENST00000392461.3:c.711-48A>G
  variant of: http://identifiers.org/hgnc/15979
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10286
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14582
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1141
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
reference allele: A

GenotypeDepth
all individuals: 554
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1831
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 146
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37393
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3123
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 567
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5003
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 606
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8453
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1198
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 885
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 970
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6326
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.553938917289291e-5
allele num: 15258
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7638
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9336
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61110
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e-1

DP
type: SiteQuality
SIO_000300: 1.607654e6

MQRankSum
type: SiteQuality
SIO_000300: -7.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.82e0

VQSLOD
type: SiteQuality
SIO_000300: 3.46e-1

QD
type: SiteQuality
SIO_000300: 1.448e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 40578
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 454
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 313
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8456
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3499
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1497
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 883
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43284
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 351
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 831
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10080
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532520076012996e-5
allele num: 65252
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11136
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16016
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8430
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.0e-1

QD
type: SiteQuality
SIO_000300: 1.216e1

DP
type: SiteQuality
SIO_000300: 1.688095e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 5.809e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.81e0

GenotypeDepth
all individuals: 972
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 796
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 233
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 876
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1035
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 454
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 922
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 20
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45120
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3763
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8465
bin: 9.75e1
variant carriers: 4

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.003842459173871e-5
allele num: 66624
num of homozygotes: 0

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

ClippingRankSum
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SIO_000300: -8.799999999999999e-2

BaseQRankSum
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SIO_000300: 2.24e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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SIO_000300: 2.7e-3

QD
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SIO_000300: 1.534e1

MQ
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SIO_000300: 5.942e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.929999999999999e-1

VQSLOD
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SIO_000300: 1.87e0

DP
type: SiteQuality
SIO_000300: 1.724501e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

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

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

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

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

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

Other
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.88e-1

VQSLOD
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ReadPosRankSum
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MQ
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DP
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MQRankSum
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SIO_000300: -3.03e-1

ClippingRankSum
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SIO_000300: -3.1e-2

InbreedingCoeff
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SIO_000300: 1.8e-3

QD
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SIO_000300: 3.37e1

BaseQRankSum
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SIO_000300: -2.371e0

GenotypeDepth
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.234e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.26e-1

MQ
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SIO_000300: 5.968e1

FS
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SIO_000300: 0.0e0

QD
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MQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

DP
type: SiteQuality
SIO_000300: 1.727188e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.11e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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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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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: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499520153550864e-5
allele num: 66688
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.418e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.234e0

InbreedingCoeff
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SIO_000300: 1.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.11e-1

VQSLOD
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ClippingRankSum
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SIO_000300: -4.26e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

DP
type: SiteQuality
SIO_000300: 1.727188e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10404
num of homozygotes: 0

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

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

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

East Asian
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allele count: 1
allele frequency: 1.158748551564311e-4
allele num: 8630
num of homozygotes: 0

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

MQRankSum
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SIO_000300: -7.83e-1

BaseQRankSum
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QD
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InbreedingCoeff
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VQSLOD
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MQ
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SIO_000300: 5.92e1

ReadPosRankSum
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FS
type: SiteQuality
SIO_000300: 9.69e-1

ClippingRankSum
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SIO_000300: -1.162e0

DP
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SIO_000300: 1.7277e6

GenotypeDepth
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variant carriers: 0

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

South Asian
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 923
bin: 7.75e1
variant carriers: 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: 8634
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQRankSum
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SIO_000300: 7.75e-1

QD
type: SiteQuality
SIO_000300: 1.078e1

VQSLOD
type: SiteQuality
SIO_000300: 5.46e-1

InbreedingCoeff
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SIO_000300: 1.29e-2

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

FS
type: SiteQuality
SIO_000300: 4.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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GenotypeDepth
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variant carriers: 8

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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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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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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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 105
allele frequency: 1.588502269288956e-2
allele num: 6610
num of homozygotes: 1

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 40
allele frequency: 5.99538355466291e-4
allele num: 66718
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 4.405286343612335e-3
allele num: 908
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.05e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 3.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.55e-2

BaseQRankSum
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SIO_000300: 8.699999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
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SIO_000300: 1.739093e6

ClippingRankSum
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SIO_000300: -3.87e-1

VQSLOD
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SIO_000300: 5.64e0

QD
type: SiteQuality
SIO_000300: 1.388e1

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10406
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: 908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -3.602e0

ReadPosRankSum
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SIO_000300: 2.24e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

MQRankSum
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DP
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SIO_000300: 1.73071e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.29e-1

QD
type: SiteQuality
SIO_000300: 2.823e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 262
bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

DP
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SIO_000300: 1.730595e6

BaseQRankSum
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SIO_000300: -3.649e0

VQSLOD
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SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.976e1

MQRankSum
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SIO_000300: 1.79e0

FS
type: SiteQuality
SIO_000300: 3.836e0

QD
type: SiteQuality
SIO_000300: 1.357e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
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bin: 9.75e1
variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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GenotypeQuality
all individuals: 912
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
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South Asian
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allele count: 1
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allele num: 16494
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.598e0

ReadPosRankSum
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SIO_000300: 1.6e0

MQRankSum
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DP
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BaseQRankSum
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SIO_000300: -5.814e0

VQSLOD
type: SiteQuality
SIO_000300: 6.13e-1

QD
type: SiteQuality
SIO_000300: 1.216e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.081e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 133

GenotypeDepth
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variant carriers: 137

GenotypeDepth
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variant carriers: 88

GenotypeDepth
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GenotypeDepth
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variant carriers: 562

GenotypeQuality
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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: 1975

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 318
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variant carriers: 1

Other
type: Population
allele count: 13
allele frequency: 1.431718061674009e-2
allele num: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1228
allele frequency: 1.841024257143714e-2
allele num: 66702
num of homozygotes: 12

South Asian
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allele count: 464
allele frequency: 2.812462116620196e-2
allele num: 16498
num of homozygotes: 15

East Asian
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allele count: 110
allele frequency: 1.27373784159333e-2
allele num: 8636
num of homozygotes: 0

European (Finnish)
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allele count: 94
allele frequency: 1.422087745839637e-2
allele num: 6610
num of homozygotes: 0

Latino
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allele count: 61
allele frequency: 5.274991352473193e-3
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num of homozygotes: 0

African
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allele count: 36
allele frequency: 3.459542571593312e-3
allele num: 10406
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.620000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

ReadPosRankSum
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DP
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VQSLOD
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SIO_000300: 4.85e0

ClippingRankSum
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SIO_000300: -2.4e-1

MQRankSum
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SIO_000300: 2.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.766e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 26
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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FS
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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DP
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QD
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VQSLOD
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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DP
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FS
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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MQ
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QD
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Latino
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Other
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MQRankSum
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MQ
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FS
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ClippingRankSum
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DP
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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East Asian
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Other
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European (Finnish)
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South Asian
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ClippingRankSum
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DP
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FS
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MQRankSum
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VQSLOD
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BaseQRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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European (Finnish)
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Other
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Latino
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African
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South Asian
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FS
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MQRankSum
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VQSLOD
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DP
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MQ
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ReadPosRankSum
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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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European (Finnish)
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African
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South Asian
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DP
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VQSLOD
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FS
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8490
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11438
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.720062208398134e-5
allele num: 10288
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16354
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66068
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.433e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

DP
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QD
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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SIO_000300: -1.008e0

BaseQRankSum
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ReadPosRankSum
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SIO_000300: -1.27e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele num: 16302
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East Asian
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allele count: 26
allele frequency: 3.08641975308642e-3
allele num: 8424
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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DP
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InbreedingCoeff
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VQSLOD
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FS
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ClippingRankSum
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ReadPosRankSum
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QD
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10228
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 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

European (Finnish)
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allele count: 0
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Latino
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allele num: 11354
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Other
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MQ
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BaseQRankSum
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FS
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ReadPosRankSum
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DP
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MQRankSum
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QD
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VQSLOD
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ClippingRankSum
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SIO_000300: -2.71e-1

InbreedingCoeff
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SIO_000300: 4.3e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16278
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10228
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.52401853206535e-5
allele num: 65616
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

East Asian
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allele count: 0
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BaseQRankSum
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SIO_000300: 2.46e0

ClippingRankSum
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MQRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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DP
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FS
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SIO_000300: 1.063e0

QD
type: SiteQuality
SIO_000300: 1.411e1

ReadPosRankSum
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SIO_000300: 5.31e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11342
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
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African
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Other
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South Asian
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East Asian
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allele num: 8366
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MQRankSum
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BaseQRankSum
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FS
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VQSLOD
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MQ
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InbreedingCoeff
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ReadPosRankSum
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QD
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DP
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65572
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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Latino
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allele frequency: 1.763357432551578e-4
allele num: 11342
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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QD
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DP
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

African
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European (Finnish)
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South Asian
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European (Non-Finnish)
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Latino
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allele num: 11328
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Other
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MQRankSum
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QD
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FS
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VQSLOD
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ReadPosRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11284
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 4
allele frequency: 6.129892420388022e-5
allele num: 65254
num of homozygotes: 0

African
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allele frequency: 9.832841691248771e-5
allele num: 10170
num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
allele num: 16226
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.942e0

ReadPosRankSum
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SIO_000300: 1.46e-1

InbreedingCoeff
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SIO_000300: 1.0e-3

FS
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QD
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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SIO_000300: -1.62e0

MQ
type: SiteQuality
SIO_000300: 5.082e1

DP
type: SiteQuality
SIO_000300: 1.639568e6

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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65306
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.157635467980295e-5
allele num: 16240
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11296
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.89e-1

QD
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MQ
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SIO_000300: 5.945e1

ReadPosRankSum
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BaseQRankSum
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FS
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DP
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MQRankSum
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SIO_000300: -1.103e0

InbreedingCoeff
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SIO_000300: 5.1e-3

VQSLOD
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SIO_000300: -3.757e0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16012
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11058
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.125586047383885e-5
allele num: 63988
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7930
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
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QD
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SIO_000300: 1.312e1

VQSLOD
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ClippingRankSum
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ReadPosRankSum
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SIO_000300: -6.0e-1

DP
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SIO_000300: 1.534655e6

MQRankSum
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SIO_000300: 3.02e0

BaseQRankSum
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SIO_000300: -1.468e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8471
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 1
allele frequency: 6.314725940894166e-5
allele num: 15836
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6452
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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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 (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 6.06e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 5.928e1

FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 4.71e-1

DP
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SIO_000300: 1.524916e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8471
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10850
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 854
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.01667344448963e-4
allele num: 9836
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62782
num of homozygotes: 0

South Asian
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allele count: 0
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InbreedingCoeff
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SIO_000300: -1.6e-3

ReadPosRankSum
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FS
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ClippingRankSum
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DP
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MQRankSum
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MQ
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VQSLOD
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BaseQRankSum
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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allele num: 812
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.311991603253739e-4
allele num: 7622
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 1
allele frequency: 6.840881105486387e-5
allele num: 14618
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58522
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InbreedingCoeff
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DP
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MQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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QD
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BaseQRankSum
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FS
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SIO_000300: 1.0782e1

ClippingRankSum
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SIO_000300: -6.820000000000001e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
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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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
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East Asian
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allele count: 6
allele frequency: 7.874015748031496e-4
allele num: 7620
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DP
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SIO_000300: 1.493951e6

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

Latino
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allele frequency: 0.0e0
allele num: 10424
num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 3.389830508474576e-5
allele num: 59000
num of homozygotes: 0

East Asian
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South Asian
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Other
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num of homozygotes: 0

InbreedingCoeff
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SIO_000300: 2.8e-3

MQRankSum
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VQSLOD
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FS
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ReadPosRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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MQ
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DP
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SIO_000300: 1.519149e6

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

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

Other
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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South Asian
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Latino
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East Asian
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European (Non-Finnish)
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BaseQRankSum
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QD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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FS
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MQRankSum
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VQSLOD
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ClippingRankSum
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DP
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SIO_000300: 1.565088e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

South Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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allele num: 59354
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

Latino
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African
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Other
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MQRankSum
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DP
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ClippingRankSum
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InbreedingCoeff
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MQ
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FS
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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QD
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GenotypeDepth
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variant carriers: 0

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

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

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

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

African
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allele frequency: 1.030290541932825e-4
allele num: 9706
num of homozygotes: 0

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

Other
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Latino
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East Asian
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African
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allele count: 7
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European (Non-Finnish)
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allele count: 0
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European (Finnish)
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VQSLOD
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MQRankSum
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ReadPosRankSum
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DP
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InbreedingCoeff
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SIO_000300: 1.0e-4

MQ
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BaseQRankSum
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FS
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6300
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.551205286507616e-5
allele num: 64466
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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East Asian
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FS
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QD
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InbreedingCoeff
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BaseQRankSum
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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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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6456
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.164415463437354e-4
allele num: 8588
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66024
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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MQ
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SIO_000300: 5.99e1

BaseQRankSum
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MQRankSum
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DP
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VQSLOD
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InbreedingCoeff
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SIO_000300: 7.0e-4

ClippingRankSum
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FS
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SIO_000300: 4.242e0

QD
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SIO_000300: 1.295e1

ReadPosRankSum
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SIO_000300: -9.28e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 2
allele frequency: 1.229709788489916e-4
allele num: 16264
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66158
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
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allele count: 0
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num of homozygotes: 0

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

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

East Asian
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allele frequency: 0.0e0
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QD
type: SiteQuality
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BaseQRankSum
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DP
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FS
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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SIO_000300: 5.75e-1

VQSLOD
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MQ
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SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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allele num: 8598
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South Asian
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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MQRankSum
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DP
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BaseQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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QD
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GenotypeDepth
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variant carriers: 0

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

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.645061728395061e-5
allele num: 10368
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

South Asian
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allele frequency: 6.141751627564181e-5
allele num: 16282
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66242
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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MQ
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DP
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FS
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MQRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

ClippingRankSum
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BaseQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

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

South Asian
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allele count: 2
allele frequency: 1.240079365079365e-4
allele num: 16128
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65864
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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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QD
type: SiteQuality
SIO_000300: 8.76e0

BaseQRankSum
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FS
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ClippingRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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DP
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SIO_000300: 1.833074e6

MQRankSum
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SIO_000300: 1.84e-1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11378
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.087538808059901e-5
allele num: 65708
num of homozygotes: 0

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

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

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

BaseQRankSum
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SIO_000300: 1.83e0

InbreedingCoeff
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SIO_000300: 4.5e-3

ReadPosRankSum
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VQSLOD
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MQRankSum
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FS
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SIO_000300: 8.186999999999999e0

ClippingRankSum
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MQ
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SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.829275e6

QD
type: SiteQuality
SIO_000300: 1.118e1

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15458
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8328
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.581727879535605e-5
allele num: 63222
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11030
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6242
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9986
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

VQSLOD
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DP
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SIO_000300: 1.765732e6

QD
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MQRankSum
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FS
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ReadPosRankSum
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SIO_000300: 9.370000000000001e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.27e-1

BaseQRankSum
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SIO_000300: -1.56e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 1.280737704918033e-4
allele num: 7808
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 10414
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59238
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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DP
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ClippingRankSum
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FS
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MQ
type: SiteQuality
SIO_000300: 5.815e1

BaseQRankSum
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QD
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SIO_000300: 1.201e1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 76
allele frequency: 5.175701443748297e-3
allele num: 14684
num of homozygotes: 2

East Asian
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allele count: 0
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num of homozygotes: 0

Latino
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allele frequency: 9.879470460383324e-5
allele num: 10122
num of homozygotes: 0

Other
type: Population
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.72717537738782e-5
allele num: 57898
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European (Finnish)
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allele count: 0
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InbreedingCoeff
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SIO_000300: 9.1e-3

MQRankSum
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QD
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DP
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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FS
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MQ
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SIO_000300: 5.988e1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5788
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9220
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.538069629210303e-5
allele num: 56528
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.068348250610252e-4
allele num: 7374
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
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InbreedingCoeff
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SIO_000300: -1.5e-3

VQSLOD
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ReadPosRankSum
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SIO_000300: 2.4e-2

FS
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SIO_000300: 9.23e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

DP
type: SiteQuality
SIO_000300: 1.546378e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.97e-1

BaseQRankSum
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SIO_000300: -2.927e0

QD
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SIO_000300: 1.221e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 467
bin: 5.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9748
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14406
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7316
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56120
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.093374152635032e-4
allele num: 9146
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5750
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQRankSum
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VQSLOD
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FS
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SIO_000300: 8.420999999999999e0

DP
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BaseQRankSum
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SIO_000300: 2.05e0

ReadPosRankSum
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SIO_000300: 1.12e0

QD
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SIO_000300: 1.247e1

MQ
type: SiteQuality
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ClippingRankSum
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SIO_000300: -1.77e-1

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.793979405116429e-5
allele num: 55742
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.095770326539557e-4
allele num: 9126
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9616
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.967670011148272e-5
allele num: 14352
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5700
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 768
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

DP
type: SiteQuality
SIO_000300: 1.525263e6

MQRankSum
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SIO_000300: 1.02e0

ClippingRankSum
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SIO_000300: 4.67e-1

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -2.1e-3

QD
type: SiteQuality
SIO_000300: 1.126e1

FS
type: SiteQuality
SIO_000300: 9.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.246e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
all individuals: 532
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54814
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14200
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.112594570538496e-4
allele num: 8988
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 756
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5628
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.934e1

ClippingRankSum
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SIO_000300: -5.56e-1

DP
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SIO_000300: 1.481681e6

MQRankSum
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FS
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SIO_000300: 0.0e0

VQSLOD
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SIO_000300: -3.328e-1

InbreedingCoeff
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SIO_000300: -2.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

QD
type: SiteQuality
SIO_000300: 1.773e1

BaseQRankSum
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SIO_000300: -2.711e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 1142
bin: 6.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6776
num of homozygotes: 0

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

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

South Asian
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allele count: 3
allele frequency: 2.16076058772688e-4
allele num: 13884
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52414
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 734
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MQRankSum
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SIO_000300: -3.87e-1

VQSLOD
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DP
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InbreedingCoeff
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BaseQRankSum
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MQ
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SIO_000300: 5.954e1

FS
type: SiteQuality
SIO_000300: 4.813e0

ClippingRankSum
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SIO_000300: -2.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.6e-2

QD
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SIO_000300: 1.02e1

GenotypeDepth
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variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.01118217288122e-5
allele num: 49722
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 706
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Latino
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.193317422434368e-4
allele num: 8380
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

South Asian
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allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 6.94e-1

BaseQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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FS
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MQ
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ClippingRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 8380
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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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: 7
allele frequency: 1.407827521016854e-4
allele num: 49722
num of homozygotes: 0

Other
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VQSLOD
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QD
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InbreedingCoeff
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MQRankSum
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FS
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DP
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ReadPosRankSum
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ClippingRankSum
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MQ
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BaseQRankSum
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SIO_000300: 1.35e-1

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5172
num of homozygotes: 0

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

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

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

South Asian
type: Population
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allele frequency: 1.498800959232614e-4
allele num: 13344
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Other
type: Population
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8172
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.310441e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.38e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

QD
type: SiteQuality
SIO_000300: 1.062e1

MQRankSum
type: SiteQuality
SIO_000300: 4.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

FS
type: SiteQuality
SIO_000300: 5.507e0

VQSLOD
type: SiteQuality
SIO_000300: 6.06e-1

GenotypeDepth
all individuals: 710
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 729
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 794
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3239
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2673
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5681
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2322
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1797
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2392
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16950
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 389
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1577
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7765
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4704
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8449
bin: 9.75e1
variant carriers: 11

GenotypeQuality
all individuals: 623
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.659313725490196e-5
allele num: 13056
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.090369853454292e-4
allele num: 45856
num of homozygotes: 0

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

African
type: Population
allele count: 4
allele frequency: 5.047955577990914e-4
allele num: 7924
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5014
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.714089818306479e-4
allele num: 5834
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.05e-1

DP
type: SiteQuality
SIO_000300: 1.295223e6

VQSLOD
type: SiteQuality
SIO_000300: 4.81e0

QD
type: SiteQuality
SIO_000300: 1.292e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

GenotypeDepth
all individuals: 1359
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 729
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 627
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2602
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8444
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 5593
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7781
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2735
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4578
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1899
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 827
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4682
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15365
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 379
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1584
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 3.112356053532524e-4
allele num: 12852
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4932
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7738
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5590
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44394
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.114000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.74e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.121e-1

QD
type: SiteQuality
SIO_000300: 1.04e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.699999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.067e0

DP
type: SiteQuality
SIO_000300: 1.285511e6

GenotypeDepth
all individuals: 888
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 195
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 593
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 338
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4472
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5996
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4214
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11343
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3274
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1972
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3594
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 519
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1690
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1772
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8664
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5588
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2356
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2753
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63600
num of homozygotes: 0