11-44958870-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44958870
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44958870
    reference: chr 11
allele count: 3
allele frequency: 2.720348204570185e-4
allele num: 11028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.306C>T
  hgvsp: ENST00000525138.1:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.222C>T
  hgvsp: ENST00000531928.2:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.222C>T
  hgvsp: ENST00000533940.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.163C>T
  hgvsp: ENSP00000437258.1:p.Arg55Trp
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.222C>T
  hgvsp: ENST00000354556.4:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.222C>T
  hgvsp: ENST00000395648.3:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.222C>T
  hgvsp: ENST00000533443.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.163C>T
  hgvsp: ENSP00000437243.1:p.Arg55Trp
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.222C>T
  hgvsp: ENST00000528473.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.222C>T
  hgvsp: ENST00000525145.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.222C>T
  hgvsp: ENST00000525680.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.410C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.222C>T
  hgvsp: ENST00000308212.5:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.422C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.222C>T
  hgvsp: ENST00000530035.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.222C>T
  hgvsp: ENST00000525683.1:c.222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.410C>T
  variant of: http://identifiers.org/hgnc/16842
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19539
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 32059
  bin: 2.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg55Trp
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-44958876-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44958876
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44958876
    reference: chr 11
allele count: 1
allele frequency: 9.266123054114158e-5
allele num: 10792
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.157C>T
  hgvsp: ENSP00000437258.1:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.216C>T
  hgvsp: ENST00000395648.3:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.216C>T
  hgvsp: ENST00000354556.4:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.216C>T
  hgvsp: ENST00000525145.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.157C>T
  hgvsp: ENSP00000437243.1:p.Leu53Phe
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.216C>T
  hgvsp: ENST00000528473.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.404C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.404C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.216C>T
  hgvsp: ENST00000533443.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.216C>T
  hgvsp: ENST00000531928.2:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.216C>T
  hgvsp: ENST00000525683.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.300C>T
  hgvsp: ENST00000525138.1:c.300C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.216C>T
  hgvsp: ENST00000308212.5:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.216C>T
  hgvsp: ENST00000527685.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.416C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.216C>T
  hgvsp: ENST00000525680.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.216C>T
  hgvsp: ENST00000530035.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.216C>T
  hgvsp: ENST00000533940.1:c.216C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18539
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu53Phe
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-44958890-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44958890
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44958890
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 10408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.143G>A
  hgvsp: ENSP00000437258.1:p.Arg48His
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.202G>A
  hgvsp: ENSP00000437284.1:p.Val68Ile
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.202G>A
  hgvsp: ENSP00000346564.4:p.Val68Ile
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.202G>A
  hgvsp: ENSP00000433454.1:p.Val68Ile
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.202G>A
  hgvsp: ENSP00000431556.1:p.Val68Ile
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.390G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.202G>A
  hgvsp: ENSP00000309532.5:p.Val68Ile
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.402G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.390G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.202G>A
  hgvsp: ENSP00000433474.1:p.Val68Ile
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.286G>A
  hgvsp: ENSP00000435739.1:p.Val96Ile
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.202G>A
  hgvsp: ENSP00000436152.1:p.Val68Ile
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.202G>A
  hgvsp: ENSP00000379009.3:p.Val68Ile
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.202G>A
  hgvsp: ENSP00000435800.1:p.Val68Ile
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.202G>A
  hgvsp: ENSP00000475501.1:p.Val68Ile
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.202G>A
  hgvsp: ENSP00000432089.1:p.Val68Ile
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.143G>A
  hgvsp: ENSP00000437243.1:p.Arg48His
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.202G>A
  hgvsp: ENSP00000434461.1:p.Val68Ile
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val68Ile
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

11-44958891-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44958891
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44958891
    reference: chr 11
allele count: 1
allele frequency: 9.674922600619196e-5
allele num: 10336
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.142C>T
  hgvsp: ENSP00000437243.1:p.Arg48Cys
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.389C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.201C>T
  hgvsp: ENST00000308212.5:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.201C>T
  hgvsp: ENST00000395648.3:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.201C>T
  hgvsp: ENST00000525145.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.201C>T
  hgvsp: ENST00000525683.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.285C>T
  hgvsp: ENST00000525138.1:c.285C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.201C>T
  hgvsp: ENST00000533443.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.201C>T
  hgvsp: ENST00000354556.4:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.142C>T
  hgvsp: ENSP00000437258.1:p.Arg48Cys
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.201C>T
  hgvsp: ENST00000525680.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.201C>T
  hgvsp: ENST00000528473.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.201C>T
  hgvsp: ENST00000530035.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.201C>T
  hgvsp: ENST00000527685.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.401C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.201C>T
  hgvsp: ENST00000533940.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.201C>T
  hgvsp: ENST00000531928.2:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.389C>T
  variant of: http://identifiers.org/hgnc/16842
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg48Cys
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ

11-44958891-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44958891
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44958891
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 10336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.201C>A
  hgvsp: ENSP00000434461.1:p.Phe67Leu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.389C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.201C>A
  hgvsp: ENSP00000437284.1:p.Phe67Leu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.201C>A
  hgvsp: ENSP00000309532.5:p.Phe67Leu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.201C>A
  hgvsp: ENSP00000432089.1:p.Phe67Leu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.201C>A
  hgvsp: ENSP00000435800.1:p.Phe67Leu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.201C>A
  hgvsp: ENSP00000379009.3:p.Phe67Leu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.201C>A
  hgvsp: ENSP00000346564.4:p.Phe67Leu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.201C>A
  hgvsp: ENSP00000436152.1:p.Phe67Leu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.389C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.201C>A
  hgvsp: ENSP00000433474.1:p.Phe67Leu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.285C>A
  hgvsp: ENSP00000435739.1:p.Phe95Leu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.201C>A
  hgvsp: ENSP00000433454.1:p.Phe67Leu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.201C>A
  hgvsp: ENSP00000475501.1:p.Phe67Leu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.201C>A
  hgvsp: ENSP00000431556.1:p.Phe67Leu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.142C>A
  hgvsp: ENSP00000437243.1:p.Arg48Ser
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.401C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.142C>A
  hgvsp: ENSP00000437258.1:p.Arg48Ser
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: missense
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe67Leu
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

11-44958892-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44958892
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44958892
    reference: chr 11
allele count: 1
allele frequency: 9.574875526618154e-5
allele num: 10444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.388T>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.141T>C
  hgvsp: ENST00000532253.1:c.141T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.200T>C
  hgvsp: ENSP00000346564.4:p.Phe67Ser
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.200T>C
  hgvsp: ENSP00000379009.3:p.Phe67Ser
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.200T>C
  hgvsp: ENSP00000434461.1:p.Phe67Ser
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.200T>C
  hgvsp: ENSP00000433454.1:p.Phe67Ser
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.388T>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.200T>C
  hgvsp: ENSP00000309532.5:p.Phe67Ser
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.200T>C
  hgvsp: ENSP00000475501.1:p.Phe67Ser
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.284T>C
  hgvsp: ENSP00000435739.1:p.Phe95Ser
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.200T>C
  hgvsp: ENSP00000437284.1:p.Phe67Ser
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.200T>C
  hgvsp: ENSP00000432089.1:p.Phe67Ser
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.400T>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.200T>C
  hgvsp: ENSP00000433474.1:p.Phe67Ser
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.200T>C
  hgvsp: ENSP00000431556.1:p.Phe67Ser
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.200T>C
  hgvsp: ENSP00000435800.1:p.Phe67Ser
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.200T>C
  hgvsp: ENSP00000436152.1:p.Phe67Ser
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.141T>C
  hgvsp: ENST00000528290.1:c.141T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe67Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-44958902-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44958902
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44958902
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 10130
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.190G>T
  hgvsp: ENSP00000437284.1:p.Val64Phe
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.190G>T
  hgvsp: ENSP00000436152.1:p.Val64Phe
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.190G>T
  hgvsp: ENSP00000433474.1:p.Val64Phe
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.190G>T
  hgvsp: ENSP00000475501.1:p.Val64Phe
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.378G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.190G>T
  hgvsp: ENSP00000309532.5:p.Val64Phe
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.190G>T
  hgvsp: ENSP00000433454.1:p.Val64Phe
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.131G>T
  hgvsp: ENSP00000437258.1:p.Gly44Val
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.378G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.190G>T
  hgvsp: ENSP00000432089.1:p.Val64Phe
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.190G>T
  hgvsp: ENSP00000346564.4:p.Val64Phe
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.190G>T
  hgvsp: ENSP00000379009.3:p.Val64Phe
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.190G>T
  hgvsp: ENSP00000431556.1:p.Val64Phe
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.274G>T
  hgvsp: ENSP00000435739.1:p.Val92Phe
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.190G>T
  hgvsp: ENSP00000434461.1:p.Val64Phe
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.390G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.190G>T
  hgvsp: ENSP00000435800.1:p.Val64Phe
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val64Phe
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

11-44958911-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44958911
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44958911
    reference: chr 11
allele count: 27
allele frequency: 2.67379679144385e-3
allele num: 10098
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.189-8C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-8C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.189-8C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.189-8C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.189-8C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.189-8C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.273-8C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-8C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.189-8C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.377-8C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.189-8C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.189-8C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.389-8C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.189-8C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.377-8C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.189-8C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.189-8C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.189-8C>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.189-8C>T
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

11-44958913-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44958913
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44958913
    reference: chr 11
allele count: 2
allele frequency: 1.992428770671449e-4
allele num: 10038
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.189-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.189-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.189-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.189-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.189-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.389-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.189-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.189-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.189-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.189-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.377-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.189-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.189-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.377-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.189-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.273-10C>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37251
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

11-44958917-AAAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44958917
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44958914
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 10076
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.189-17_189-15delCTT
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.189-17_189-15delCTT
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.189-17_189-15delCTT
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.189-17_189-15delCTT
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.189-17_189-15delCTT
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.189-17_189-15delCTT
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.189-17_189-15delCTT
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.189-17_189-15delCTT
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-17_130-15delCTT
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.377-17_377-15delCTT
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-17_130-15delCTT
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.377-17_377-15delCTT
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.273-17_273-15delCTT
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.189-17_189-15delCTT
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.189-17_189-15delCTT
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.389-17_389-15delCTT
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.189-17_189-15delCTT
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.189-17_189-15delCTT
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: AAAG
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

11-44958932-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44958932
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44958932
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 9988
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.189-29G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.189-29G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.189-29G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.389-29G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.189-29G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.189-29G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.189-29G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.377-29G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.189-29G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.189-29G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.189-29G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.377-29G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-29G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-29G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.273-29G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.189-29G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.189-29G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.189-29G>A
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

11-44958936-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44958936
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44958936
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 9956
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.273-33G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.189-33G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.189-33G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.189-33G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.189-33G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.189-33G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.189-33G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.189-33G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.189-33G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.189-33G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.189-33G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-33G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.189-33G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.189-33G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.377-33G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.377-33G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-33G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.389-33G>A
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11696
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-44959056-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959056
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959056
    reference: chr 11
allele count: 1
allele frequency: 9.066840750009067e-6
allele num: 110292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.376+50G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.388+50G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.188+50G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.188+50G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-153G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.188+50G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.188+50G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.188+50G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-153G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.188+50G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.188+50G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.188+50G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.272+50G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.188+50G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.188+50G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.188+50G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.376+50G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.188+50G>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14694
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

11-44959056-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959056
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959056
    reference: chr 11
allele count: 2
allele frequency: 1.813368150001813e-5
allele num: 110292
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.188+50G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-153G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.388+50G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.188+50G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.188+50G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.188+50G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.188+50G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.188+50G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.188+50G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.376+50G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.188+50G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.188+50G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.188+50G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.188+50G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-153G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.188+50G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.272+50G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.376+50G>A
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11830
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7508
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

11-44959059-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959059
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959059
    reference: chr 11
allele count: 1
allele frequency: 9.019735180575098e-6
allele num: 110868
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.188+47T>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.188+47T>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.376+47T>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.188+47T>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.376+47T>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.388+47T>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.272+47T>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.188+47T>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-156T>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.188+47T>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.188+47T>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-156T>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.188+47T>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.188+47T>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.188+47T>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.188+47T>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.188+47T>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.188+47T>A
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/11-44959061-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959061
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959061
    reference: chr 11
allele count: 8758
allele frequency: 7.910329130387658e-2
allele num: 110716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.188+45G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.376+45G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.188+45G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-158G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.188+45G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.188+45G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.188+45G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.188+45G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.188+45G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.388+45G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.188+45G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.188+45G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-158G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.188+45G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.376+45G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.188+45G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.188+45G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.272+45G>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 7.5e0
  variant carriers: 263
genotype depth: GenotypeDepth
  all individuals: 15912
  bin: 2.25e1
  variant carriers: 2049
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 30
genotype quality: GenotypeQuality
num of homozygotes: 418
population: Other
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-44959061-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959061
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959061
    reference: chr 11
allele count: 3
allele frequency: 2.709635463708949e-5
allele num: 110716
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.188+45G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-158G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.188+45G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.188+45G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.376+45G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.188+45G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.188+45G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.272+45G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.188+45G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.188+45G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.188+45G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-158G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.188+45G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.188+45G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.188+45G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.376+45G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.188+45G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.388+45G>A
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15912
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11019
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-44959062-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959062
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959062
    reference: chr 11
allele count: 3
allele frequency: 2.692998204667864e-5
allele num: 111400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-159C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.188+44C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.188+44C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.188+44C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.376+44C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.188+44C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.272+44C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.188+44C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.188+44C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-159C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.188+44C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.188+44C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.188+44C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.376+44C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.188+44C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.188+44C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.388+44C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.188+44C>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17571
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9036
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

11-44959064-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959064
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959064
    reference: chr 11
allele count: 12
allele frequency: 1.072788714262726e-4
allele num: 111858
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-161G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.188+42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.188+42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.188+42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.188+42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.188+42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.388+42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.188+42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.188+42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.188+42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.376+42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.188+42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.272+42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.188+42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.188+42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.376+42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.188+42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-161G>A
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 796
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

11-44959065-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959065
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959065
    reference: chr 11
allele count: 7
allele frequency: 6.283549666971868e-5
allele num: 111402
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.188+41C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.188+41C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.376+41C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.188+41C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.376+41C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.188+41C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.188+41C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.272+41C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.188+41C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.188+41C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.188+41C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-162C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-162C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.188+41C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.188+41C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.188+41C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.188+41C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.388+41C>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6370
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/11-44959066-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959066
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959066
    reference: chr 11
allele count: 4
allele frequency: 3.563791874554526e-5
allele num: 112240
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.272+40G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.188+40G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.188+40G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.376+40G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-163G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.188+40G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.188+40G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.188+40G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-163G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.188+40G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.188+40G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.388+40G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.188+40G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.188+40G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.188+40G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.376+40G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.188+40G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.188+40G>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21087
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9877
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-44959070-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959070
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959070
    reference: chr 11
allele count: 1
allele frequency: 8.874059349708931e-6
allele num: 112688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.188+36G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.388+36G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.376+36G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.188+36G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.188+36G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.188+36G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.188+36G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-167G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.376+36G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.188+36G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.188+36G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.188+36G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.188+36G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.188+36G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.188+36G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.272+36G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-167G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.188+36G>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-44959081-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959081
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959081
    reference: chr 11
allele count: 33
allele frequency: 2.887088589875943e-4
allele num: 114302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.376+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.188+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.188+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.188+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.188+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.188+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-178G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-178G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.388+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.188+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.376+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.188+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.272+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.188+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.188+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.188+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.188+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.188+25G>A
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27430
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

11-44959082-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959082
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959082
    reference: chr 11
allele count: 3
allele frequency: 2.620361959331982e-5
allele num: 114488
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-179G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.188+24G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.188+24G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.376+24G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.188+24G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.388+24G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.272+24G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.188+24G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.188+24G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.188+24G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.188+24G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.188+24G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-179G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.188+24G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.188+24G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.188+24G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.188+24G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.376+24G>C
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27607
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-44959083-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959083
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959083
    reference: chr 11
allele count: 1
allele frequency: 8.560764305037153e-6
allele num: 116812
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.376+23G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.188+23G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.188+23G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-180G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.188+23G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.388+23G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.188+23G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-180G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.188+23G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.188+23G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.376+23G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.188+23G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.188+23G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.272+23G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.188+23G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.188+23G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.188+23G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.188+23G>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19555
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ

11-44959083-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959083
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959083
    reference: chr 11
allele count: 28965
allele frequency: 2.479625380954012e-1
allele num: 116812
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.188+23G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.188+23G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.188+23G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-180G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.188+23G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.188+23G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.188+23G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.188+23G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.188+23G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.376+23G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.188+23G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-180G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.188+23G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.188+23G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.272+23G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.188+23G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.376+23G>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.388+23G>C
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 13554
  bin: 2.75e1
  variant carriers: 4884
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 1.75e1
  variant carriers: 2862
genotype depth: GenotypeDepth
  all individuals: 2861
  bin: 1.25e1
  variant carriers: 1151
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 4.75e1
  variant carriers: 931
genotype quality: GenotypeQuality
num of homozygotes: 4334
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/11-44959084-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959084
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959084
    reference: chr 11
allele count: 4
allele frequency: 3.405182688051214e-5
allele num: 117468
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.188+22T>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.188+22T>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.188+22T>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.188+22T>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.188+22T>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.188+22T>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.376+22T>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.188+22T>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.376+22T>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.188+22T>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.388+22T>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.188+22T>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-181T>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.188+22T>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.188+22T>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.188+22T>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.272+22T>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-181T>G
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2789
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7417
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

11-44959099-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959099
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959099
    reference: chr 11
allele count: 1
allele frequency: 8.460666362082677e-6
allele num: 118194
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.188+7A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.188+7A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.188+7A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.188+7A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.188+7A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.388+7A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.188+7A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.376+7A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.188+7A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.188+7A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.376+7A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.188+7A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.188+7A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.188+7A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-196A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.188+7A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.272+7A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-196A>G
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.188+7A>G
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

11-44959100-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959100
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959100
    reference: chr 11
allele count: 3
allele frequency: 2.537813419957365e-5
allele num: 118212
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.376+6C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.188+6C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.272+6C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-197C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.188+6C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.188+6C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-197C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.188+6C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.188+6C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.188+6C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.188+6C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.376+6C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.188+6C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.188+6C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.388+6C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.188+6C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.188+6C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.188+6C>A
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22604
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.188+6C>A
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

11-44959111-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959111
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959111
    reference: chr 11
allele count: 1
allele frequency: 8.432983083435934e-6
allele num: 118582
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-208G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.183G>A
  hgvsp: ENST00000395648.3:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.183G>A
  hgvsp: ENST00000533443.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.383G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.183G>A
  hgvsp: ENST00000308212.5:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.183G>A
  hgvsp: ENST00000533937.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.371G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.267G>A
  hgvsp: ENST00000525138.1:c.267G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.183G>A
  hgvsp: ENST00000531928.2:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.183G>A
  hgvsp: ENST00000525683.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.183G>A
  hgvsp: ENST00000525145.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.183G>A
  hgvsp: ENST00000528473.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.183G>A
  hgvsp: ENST00000530035.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.183G>A
  hgvsp: ENST00000354556.4:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.183G>A
  hgvsp: ENST00000527685.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-208G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.371G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.183G>A
  hgvsp: ENST00000533940.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.183G>A
  hgvsp: ENST00000525680.1:c.183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly61Gly
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

11-44959116-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959116
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959116
    reference: chr 11
allele count: 13
allele frequency: 1.094976584346889e-4
allele num: 118724
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.178T>C
  hgvsp: ENST00000525145.1:c.178T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.178T>C
  hgvsp: ENST00000525683.1:c.178T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-213T>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.378T>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.178T>C
  hgvsp: ENST00000527685.1:c.178T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.178T>C
  hgvsp: ENST00000533443.1:c.178T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.178T>C
  hgvsp: ENST00000395648.3:c.178T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-213T>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.178T>C
  hgvsp: ENST00000528473.1:c.178T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.262T>C
  hgvsp: ENST00000525138.1:c.262T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.178T>C
  hgvsp: ENST00000531928.2:c.178T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.178T>C
  hgvsp: ENST00000533937.1:c.178T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.366T>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.178T>C
  hgvsp: ENST00000525680.1:c.178T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.178T>C
  hgvsp: ENST00000530035.1:c.178T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.366T>C
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.178T>C
  hgvsp: ENST00000354556.4:c.178T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.178T>C
  hgvsp: ENST00000308212.5:c.178T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.178T>C
  hgvsp: ENST00000533940.1:c.178T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Leu60Leu
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

11-44959128-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959128
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959128
    reference: chr 11
allele count: 1
allele frequency: 8.410146000134562e-6
allele num: 118904
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.166A>G
  hgvsp: ENSP00000435800.1:p.Ile56Val
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.166A>G
  hgvsp: ENSP00000346564.4:p.Ile56Val
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.166A>G
  hgvsp: ENSP00000433474.1:p.Ile56Val
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.166A>G
  hgvsp: ENSP00000437284.1:p.Ile56Val
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.354A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.250A>G
  hgvsp: ENSP00000435739.1:p.Ile84Val
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.166A>G
  hgvsp: ENSP00000432089.1:p.Ile56Val
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.166A>G
  hgvsp: ENSP00000434461.1:p.Ile56Val
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.166A>G
  hgvsp: ENSP00000432926.1:p.Ile56Val
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.166A>G
  hgvsp: ENSP00000431556.1:p.Ile56Val
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.166A>G
  hgvsp: ENSP00000433454.1:p.Ile56Val
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.166A>G
  hgvsp: ENSP00000379009.3:p.Ile56Val
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.366A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-225A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.166A>G
  hgvsp: ENSP00000309532.5:p.Ile56Val
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.166A>G
  hgvsp: ENSP00000475501.1:p.Ile56Val
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.166A>G
  hgvsp: ENSP00000436152.1:p.Ile56Val
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.354A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-225A>G
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ile56Val
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-44959129-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959129
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959129
    reference: chr 11
allele count: 2
allele frequency: 1.682029200026912e-5
allele num: 118904
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.165C>T
  hgvsp: ENST00000308212.5:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.165C>T
  hgvsp: ENST00000527685.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-226C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.165C>T
  hgvsp: ENST00000395648.3:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.165C>T
  hgvsp: ENST00000525145.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.165C>T
  hgvsp: ENST00000533937.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.165C>T
  hgvsp: ENST00000354556.4:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.365C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.353C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.165C>T
  hgvsp: ENST00000533443.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.165C>T
  hgvsp: ENST00000525680.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.165C>T
  hgvsp: ENST00000528473.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.165C>T
  hgvsp: ENST00000533940.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.165C>T
  hgvsp: ENST00000525683.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.165C>T
  hgvsp: ENST00000530035.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.353C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.165C>T
  hgvsp: ENST00000531928.2:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.249C>T
  hgvsp: ENST00000525138.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-226C>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Thr55Thr
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD

11-44959135-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959135
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959135
    reference: chr 11
allele count: 2
allele frequency: 1.681972617485787e-5
allele num: 118908
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.159G>A
  hgvsp: ENST00000533940.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.159G>A
  hgvsp: ENST00000308212.5:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.359G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-232G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.159G>A
  hgvsp: ENST00000533937.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.159G>A
  hgvsp: ENST00000525683.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.159G>A
  hgvsp: ENST00000530035.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.347G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.159G>A
  hgvsp: ENST00000533443.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.159G>A
  hgvsp: ENST00000354556.4:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.347G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.243G>A
  hgvsp: ENST00000525138.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.159G>A
  hgvsp: ENST00000527685.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-232G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.159G>A
  hgvsp: ENST00000531928.2:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.159G>A
  hgvsp: ENST00000525145.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.159G>A
  hgvsp: ENST00000395648.3:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.159G>A
  hgvsp: ENST00000528473.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.159G>A
  hgvsp: ENST00000525680.1:c.159G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Lys53Lys
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

11-44959153-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959153
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959153
    reference: chr 11
allele count: 1
allele frequency: 8.424599831508003e-6
allele num: 118700
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.141C>T
  hgvsp: ENST00000533940.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.141C>T
  hgvsp: ENST00000527685.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.141C>T
  hgvsp: ENST00000525145.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-250C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.141C>T
  hgvsp: ENST00000525680.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.141C>T
  hgvsp: ENST00000528473.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.141C>T
  hgvsp: ENST00000308212.5:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.141C>T
  hgvsp: ENST00000530035.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.141C>T
  hgvsp: ENST00000525683.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.141C>T
  hgvsp: ENST00000395648.3:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.141C>T
  hgvsp: ENST00000533443.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.141C>T
  hgvsp: ENST00000533937.1:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.225C>T
  hgvsp: ENST00000525138.1:c.225C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.141C>T
  hgvsp: ENST00000531928.2:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.141C>T
  hgvsp: ENST00000354556.4:c.141C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-250C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.329C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.329C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.341C>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Val47Val
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

11-44959162-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959162
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959162
    reference: chr 11
allele count: 50
allele frequency: 4.216633776923207e-4
allele num: 118578
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.320C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-259C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.216C>A
  hgvsp: ENST00000525138.1:c.216C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.132C>A
  hgvsp: ENST00000528473.1:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.320C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.132C>A
  hgvsp: ENST00000525145.1:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.132C>A
  hgvsp: ENST00000525680.1:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.132C>A
  hgvsp: ENST00000354556.4:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.132C>A
  hgvsp: ENST00000308212.5:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.132C>A
  hgvsp: ENST00000525683.1:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.132C>A
  hgvsp: ENST00000531928.2:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.132C>A
  hgvsp: ENST00000533443.1:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.132C>A
  hgvsp: ENST00000395648.3:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.332C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-259C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.132C>A
  hgvsp: ENST00000530035.1:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.132C>A
  hgvsp: ENST00000533940.1:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.132C>A
  hgvsp: ENST00000533937.1:c.132C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.132C>A
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum

11-44959174-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959174
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959174
    reference: chr 11
allele count: 1
allele frequency: 8.457517887650332e-6
allele num: 118238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.130-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.130-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.130-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.130-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.318-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.130-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.214-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.130-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-271C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.318-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.330-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.130-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.130-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.130-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.130-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.130-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-271C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.130-10C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.130-10C>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3963
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7352
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

11-44959178-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959178
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959178
    reference: chr 11
allele count: 2
allele frequency: 1.691703884152118e-5
allele num: 118224
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.130-14C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.130-14C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.130-14C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.214-14C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.130-14C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.130-14C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-275C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.130-14C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.130-14C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.130-14C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.130-14C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.130-14C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.318-14C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.318-14C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.130-14C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.330-14C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-275C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.130-14C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.130-14C>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7299
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18775
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum

11-44959179-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959179
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959179
    reference: chr 11
allele count: 12
allele frequency: 1.015503351161059e-4
allele num: 118168
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.130-15C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.214-15C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.130-15C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.130-15C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-276C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.130-15C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.130-15C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.130-15C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.130-15C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.330-15C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.130-15C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.130-15C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.130-15C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.130-15C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.130-15C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.318-15C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.318-15C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.130-15C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-276C>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-44959186-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959186
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959186
    reference: chr 11
allele count: 1
allele frequency: 8.475007203756124e-6
allele num: 117994
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.130-22C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.130-22C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.318-22C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.214-22C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.130-22C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.130-22C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.330-22C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.130-22C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.130-22C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.130-22C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-283C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.130-22C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.130-22C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.130-22C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.130-22C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.130-22C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-283C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.318-22C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.130-22C>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

11-44959195-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959195
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959195
    reference: chr 11
allele count: 1
allele frequency: 8.512232077495362e-6
allele num: 117478
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.130-31C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-292C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.130-31C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.130-31C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.130-31C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.130-31C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.130-31C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.130-31C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.130-31C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.318-31C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.330-31C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.130-31C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.130-31C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.214-31C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.130-31C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.318-31C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.130-31C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-292C>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.130-31C>A
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15391
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-44959202-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959202
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959202
    reference: chr 11
allele count: 1
allele frequency: 8.570155291213876e-6
allele num: 116684
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-299C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.318-38C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.330-38C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.130-38C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.130-38C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.130-38C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.130-38C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.130-38C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.130-38C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.130-38C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-299C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.130-38C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.214-38C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.318-38C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.130-38C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.130-38C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.130-38C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.130-38C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.130-38C>G
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/11-44959206-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959206
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959206
    reference: chr 11
allele count: 8905
allele frequency: 7.674739291562527e-2
allele num: 116030
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.318-42G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-303G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.130-42G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.130-42G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.130-42G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.130-42G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.130-42G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-303G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.214-42G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.130-42G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.130-42G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.130-42G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.130-42G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.130-42G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.130-42G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.130-42G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.318-42G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.330-42G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.130-42G>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5916
  bin: 3.25e1
  variant carriers: 1174
genotype depth: GenotypeDepth
  all individuals: 12195
  bin: 1.75e1
  variant carriers: 1363
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.25e1
  variant carriers: 389
genotype quality: GenotypeQuality
num of homozygotes: 431
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS

11-44959206-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959206
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959206
    reference: chr 11
allele count: 2
allele frequency: 1.723692148582263e-5
allele num: 116030
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.130-42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.214-42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.130-42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.130-42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-303G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.130-42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.130-42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.130-42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.330-42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.130-42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.130-42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.130-42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-303G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.318-42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.130-42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.130-42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.130-42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.318-42G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.130-42G>A
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11256
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

11-44959212-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959212
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959212
    reference: chr 11
allele count: 1
allele frequency: 8.692024198595368e-6
allele num: 115048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.130-48C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.318-48C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.130-48C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.330-48C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.130-48C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.318-48C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.130-48C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.130-48C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.130-48C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.130-48C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.130-48C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.130-48C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-309C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.130-48C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-309C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.130-48C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.130-48C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.130-48C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.214-48C>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14880
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10881
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

11-44959213-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959213
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959213
    reference: chr 11
allele count: 53480
allele frequency: 4.724965985192515e-1
allele num: 113186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-310G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.130-49G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.214-49G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.130-49G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.130-49G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.130-49G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.130-49G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.330-49G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.130-49G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.130-49G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-310G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.318-49G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.130-49G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.130-49G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.130-49G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.130-49G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.130-49G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.318-49G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.130-49G>A
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 9.75e1
  variant carriers: 312
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 13609
  bin: 2.25e1
  variant carriers: 9627
genotype quality: GenotypeQuality
num of homozygotes: 12948
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

11-44959215-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959215
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959215
    reference: chr 11
allele count: 1
allele frequency: 8.797550761867896e-6
allele num: 113668
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.214-51G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.130-312G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.130-51G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.130-51G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.130-51G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.130-51G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.130-51G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.130-312G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.130-51G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.318-51G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.130-51G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.130-51G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.130-51G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.130-51G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.130-51G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.130-51G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.330-51G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.318-51G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.130-51G>A
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8747
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

11-44959714-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959714
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959714
    reference: chr 11
allele count: 18
allele frequency: 1.974680211510192e-4
allele num: 91154
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.329+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.129+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.129+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.129+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.129+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.129+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.129+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.129+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.317+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.129+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.129+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.129+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.129+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.129+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.317+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.129+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.213+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.129+44A>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.129+44A>G
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11090
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

11-44959717-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959717
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959717
    reference: chr 11
allele count: 8
allele frequency: 8.749097749294605e-5
allele num: 91438
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.129+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.129+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.329+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.129+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.129+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.129+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.129+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.129+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.129+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.129+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.129+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.317+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.213+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.129+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.129+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.317+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.129+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.129+41G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.129+41G>A
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

11-44959722-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959722
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959722
    reference: chr 11
allele count: 1
allele frequency: 1.083611460274804e-5
allele num: 92284
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.129+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.129+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.129+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.329+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.129+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.213+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.129+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.129+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.129+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.129+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.129+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.129+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.129+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.129+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.129+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.129+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.129+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.317+36G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.317+36G>A
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3193
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/11-44959732-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959732
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959732
    reference: chr 11
allele count: 1
allele frequency: 1.060332944544587e-5
allele num: 94310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.129+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.129+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.129+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.129+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.129+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.129+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.129+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.129+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.129+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.317+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.213+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.129+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.129+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.129+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.129+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.129+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.317+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.129+26G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.329+26G>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

11-44959733-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959733
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959733
    reference: chr 11
allele count: 2
allele frequency: 2.10743714568713e-5
allele num: 94902
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.329+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.129+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.129+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.317+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.129+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.129+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.213+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.129+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.129+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.129+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.129+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.317+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.129+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.129+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.129+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.129+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.129+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.129+25G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.129+25G>A
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13440
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

11-44959734-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959734
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959734
    reference: chr 11
allele count: 3
allele frequency: 3.147359365492352e-5
allele num: 95318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.129+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.129+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.129+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.317+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.129+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.129+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.129+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.129+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.213+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.129+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.129+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.329+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.129+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.129+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.129+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.129+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.129+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.317+24C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.129+24C>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-44959740-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959740
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959740
    reference: chr 11
allele count: 3
allele frequency: 3.053310806684715e-5
allele num: 98254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.129+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.213+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.317+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.329+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.129+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.129+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.129+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.129+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.129+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.129+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.129+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.129+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.129+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.129+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.129+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.129+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.129+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.317+18G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.129+18G>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9424
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

11-44959741-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959741
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959741
    reference: chr 11
allele count: 1
allele frequency: 1.013007010008509e-5
allele num: 98716
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.129+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.129+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.213+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.129+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.129+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.129+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.129+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.317+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.129+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.129+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.129+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.317+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.329+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.129+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.129+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.129+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.129+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.129+17G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.129+17G>A
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2348
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-44959742-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959742
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959742
    reference: chr 11
allele count: 1
allele frequency: 1.010060199587895e-5
allele num: 99004
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.317+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.317+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.129+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.129+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.129+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.129+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.129+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.129+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.129+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.213+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.129+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.129+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.129+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.129+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.129+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.129+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.129+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.129+16G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.329+16G>A
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30535
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-44959749-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959749
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959749
    reference: chr 11
allele count: 1
allele frequency: 9.841357320001574e-6
allele num: 101612
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.129+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.129+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.129+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.317+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.129+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.129+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.213+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.129+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.129+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.129+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.129+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.129+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.129+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.129+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.129+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.129+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.329+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.317+9C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.129+9C>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-44959752-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959752
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959752
    reference: chr 11
allele count: 1
allele frequency: 9.728383531792358e-6
allele num: 102792
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.129+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.129+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.129+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.129+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.129+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.129+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.129+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.129+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.317+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.213+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.129+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.129+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.129+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.129+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.129+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.129+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.317+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.129+6G>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.329+6G>T
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: c.129+6G>T
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

11-44959761-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959761
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959761
    reference: chr 11
allele count: 1
allele frequency: 9.471490812653911e-6
allele num: 105580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.126C>T
  hgvsp: ENST00000308212.5:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.314C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.126C>T
  hgvsp: ENST00000533443.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.126C>T
  hgvsp: ENST00000525683.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.126C>T
  hgvsp: ENST00000533937.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.126C>T
  hgvsp: ENST00000532253.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.126C>T
  hgvsp: ENST00000528290.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.126C>T
  hgvsp: ENST00000525145.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.126C>T
  hgvsp: ENST00000531928.2:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.210C>T
  hgvsp: ENST00000525138.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.126C>T
  hgvsp: ENST00000395648.3:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.126C>T
  hgvsp: ENST00000530035.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.126C>T
  hgvsp: ENST00000527685.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.126C>T
  hgvsp: ENST00000525680.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.126C>T
  hgvsp: ENST00000528473.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.326C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.126C>T
  hgvsp: ENST00000533940.1:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.314C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.126C>T
  hgvsp: ENST00000354556.4:c.126C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Ser42Ser
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

11-44959776-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959776
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959776
    reference: chr 11
allele count: 57
allele frequency: 5.278168753240981e-4
allele num: 107992
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.111G>A
  hgvsp: ENST00000525683.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.195G>A
  hgvsp: ENST00000525138.1:c.195G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.111G>A
  hgvsp: ENST00000354556.4:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.111G>A
  hgvsp: ENST00000527685.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.299G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.111G>A
  hgvsp: ENST00000525145.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.111G>A
  hgvsp: ENST00000533443.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.111G>A
  hgvsp: ENST00000530035.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.111G>A
  hgvsp: ENST00000528473.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.111G>A
  hgvsp: ENST00000528290.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.111G>A
  hgvsp: ENST00000531928.2:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.111G>A
  hgvsp: ENST00000533940.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.111G>A
  hgvsp: ENST00000532253.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.111G>A
  hgvsp: ENST00000525680.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.111G>A
  hgvsp: ENST00000533937.1:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.111G>A
  hgvsp: ENST00000395648.3:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.311G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.299G>A
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.111G>A
  hgvsp: ENST00000308212.5:c.111G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Gly37Gly
num of homozygotes: 2
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

11-44959779-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959779
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959779
    reference: chr 11
allele count: 3
allele frequency: 2.773207121595888e-5
allele num: 108178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.108C>T
  hgvsp: ENST00000525680.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.192C>T
  hgvsp: ENST00000525138.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.108C>T
  hgvsp: ENST00000525683.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.308C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.108C>T
  hgvsp: ENST00000533443.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.108C>T
  hgvsp: ENST00000533937.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.108C>T
  hgvsp: ENST00000531928.2:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.108C>T
  hgvsp: ENST00000530035.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.108C>T
  hgvsp: ENST00000527685.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.108C>T
  hgvsp: ENST00000533940.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.108C>T
  hgvsp: ENST00000354556.4:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.108C>T
  hgvsp: ENST00000308212.5:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.296C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.108C>T
  hgvsp: ENST00000532253.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.108C>T
  hgvsp: ENST00000395648.3:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.108C>T
  hgvsp: ENST00000528473.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.108C>T
  hgvsp: ENST00000528290.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.296C>T
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.108C>T
  hgvsp: ENST00000525145.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
genotype quality: GenotypeQuality
hgvs: p.Asp36Asp
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

11-44959779-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 44959779
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 44959779
    reference: chr 11
allele count: 3
allele frequency: 2.773207121595888e-5
allele num: 108178
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435739
  ensembl transcript: ENST00000525138
  gene symbol: TP53I11
  hgvsc: ENST00000525138.1:c.192C>G
  hgvsp: ENSP00000435739.1:p.Asp64Glu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432089
  ensembl transcript: ENST00000530035
  gene symbol: TP53I11
  hgvsc: ENST00000530035.1:c.108C>G
  hgvsp: ENSP00000432089.1:p.Asp36Glu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000531130
  gene symbol: TP53I11
  hgvsc: ENST00000531130.2:n.308C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000432926
  ensembl transcript: ENST00000533937
  gene symbol: TP53I11
  hgvsc: ENST00000533937.1:c.108C>G
  hgvsp: ENSP00000432926.1:p.Asp36Glu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000431556
  ensembl transcript: ENST00000527685
  gene symbol: TP53I11
  hgvsc: ENST00000527685.1:c.108C>G
  hgvsp: ENSP00000431556.1:p.Asp36Glu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000435800
  ensembl transcript: ENST00000525145
  gene symbol: TP53I11
  hgvsc: ENST00000525145.1:c.108C>G
  hgvsp: ENSP00000435800.1:p.Asp36Glu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000436152
  ensembl transcript: ENST00000533940
  gene symbol: TP53I11
  hgvsc: ENST00000533940.1:c.108C>G
  hgvsp: ENSP00000436152.1:p.Asp36Glu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000532921
  gene symbol: TP53I11
  hgvsc: ENST00000532921.1:n.296C>G
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433454
  ensembl transcript: ENST00000528473
  gene symbol: TP53I11
  hgvsc: ENST00000528473.1:c.108C>G
  hgvsp: ENSP00000433454.1:p.Asp36Glu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437243
  ensembl transcript: ENST00000532253
  gene symbol: TP53I11
  hgvsc: ENST00000532253.1:c.108C>G
  hgvsp: ENSP00000437243.1:p.Asp36Glu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437284
  ensembl transcript: ENST00000533443
  gene symbol: TP53I11
  hgvsc: ENST00000533443.1:c.108C>G
  hgvsp: ENSP00000437284.1:p.Asp36Glu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000309532
  ensembl transcript: ENST00000308212
  gene symbol: TP53I11
  hgvsc: ENST00000308212.5:c.108C>G
  hgvsp: ENSP00000309532.5:p.Asp36Glu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000379009
  ensembl transcript: ENST00000395648
  gene symbol: TP53I11
  hgvsc: ENST00000395648.3:c.108C>G
  hgvsp: ENSP00000379009.3:p.Asp36Glu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000434461
  ensembl transcript: ENST00000525683
  gene symbol: TP53I11
  hgvsc: ENST00000525683.1:c.108C>G
  hgvsp: ENSP00000434461.1:p.Asp36Glu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000346564
  ensembl transcript: ENST00000354556
  gene symbol: TP53I11
  hgvsc: ENST00000354556.4:c.108C>G
  hgvsp: ENSP00000346564.4:p.Asp36Glu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000437258
  ensembl transcript: ENST00000528290
  gene symbol: TP53I11
  hgvsc: ENST00000528290.1:c.108C>G
  hgvsp: ENSP00000437258.1:p.Asp36Glu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000433474
  ensembl transcript: ENST00000525680
  gene symbol: TP53I11
  hgvsc: ENST00000525680.1:c.108C>G
  hgvsp: ENSP00000433474.1:p.Asp36Glu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000175274
  ensembl protein: ENSP00000475501
  ensembl transcript: ENST00000531928
  gene symbol: TP53I11
  hgvsc: ENST00000531928.2:c.108C>G
  hgvsp: ENSP00000475501.1:p.Asp36Glu
  variant of: http://identifiers.org/hgnc/16842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000175274
  ensembl transcript: ENST00000533955
  gene symbol: TP53I11
  hgvsc: ENST00000533955.1:n.296C>G
  variant of: http://identifiers.org/hgnc/16842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
hgvs: p.Asp36Glu
num of homozygotes: 1
reference allele: G

GenotypeDepth
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1507
bin: 1.25e1
variant carriers: 2

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

GenotypeDepth
all individuals: 2438
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 328
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 4.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1
bin: 7.25e1
variant carriers: 0

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

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

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

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31091
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1631
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2758
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17026
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 227
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1706
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 41
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 199
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 1.25e1
variant carriers: 3

GenotypeQuality
all individuals: 204
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 9.75e1
variant carriers: 3

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2470
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.634521085322001e-4
allele num: 6118
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.656967840735069e-4
allele num: 1306
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 86
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.557632398753894e-3
allele num: 642
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.111e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

FS
type: SiteQuality
SIO_000300: 1.26e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.23e-1

DP
type: SiteQuality
SIO_000300: 3.3394e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.02e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.23e-1

GenotypeDepth
all individuals: 331
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 103
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1293
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2425
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 33087
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1237
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 74
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1480
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 31780
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2734
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14689
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1704
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2812
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2458
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6132
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 78
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.416195856873823e-4
allele num: 1062
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

DP
type: SiteQuality
SIO_000300: 3.26731e5

FS
type: SiteQuality
SIO_000300: 8.75e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.02e0

VQSLOD
type: SiteQuality
SIO_000300: -1.935e0

QD
type: SiteQuality
SIO_000300: 1.135e1

MQRankSum
type: SiteQuality
SIO_000300: 5.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.16e-2

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

GenotypeDepth
all individuals: 34602
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1064
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16827
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 2452
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1254
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 100
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 334
bin: 3.25e1
variant carriers: 0

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

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

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

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

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2318
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1773
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 2.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 140
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33347
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2773
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 629
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12706
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6148
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2454
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 714
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.44e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

DP
type: SiteQuality
SIO_000300: 3.17009e5

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

QD
type: SiteQuality
SIO_000300: 8.859999999999999e0

GenotypeDepth
all individuals: 2456
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

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

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

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

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

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

GenotypeDepth
all individuals: 1
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 102
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1046
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 34913
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 16464
bin: 7.5e0
variant carriers: 2

GenotypeDepth
all individuals: 334
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33584
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12113
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2437
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2074
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 209
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2777
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 76
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 127
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.084967320261438e-4
allele num: 2448
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6130
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 684
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-2

QD
type: SiteQuality
SIO_000300: 1.164e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

FS
type: SiteQuality
SIO_000300: 1.734e0

DP
type: SiteQuality
SIO_000300: 3.15023e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 102
bin: 1.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 6
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 34913
bin: 2.5e0
variant carriers: 1

GenotypeDepth
all individuals: 16464
bin: 7.5e0
variant carriers: 2

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

GenotypeDepth
all individuals: 334
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2456
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1254
bin: 2.75e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 232
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 233
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1861
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33584
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12113
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2074
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2437
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2777
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 320
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6130
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2448
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.15023e5

MQRankSum
type: SiteQuality
SIO_000300: -2.26e-1

FS
type: SiteQuality
SIO_000300: 1.734e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.164e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

GenotypeDepth
all individuals: 16468
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1254
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 335
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 6.25e1
variant carriers: 0

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

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

GenotypeDepth
all individuals: 34973
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2465
bin: 2.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1021
bin: 1.25e1
variant carriers: 0

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

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

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

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

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

GenotypeQuality
all individuals: 2795
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12531
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 237
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1723
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33810
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1830
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 127
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2203
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 210
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 700
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 332
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.058441558441559e-4
allele num: 2464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6180
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.38e1

VQSLOD
type: SiteQuality
SIO_000300: -1.724e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.84e-1

DP
type: SiteQuality
SIO_000300: 3.15314e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.419999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.87e0

Annotation
canonical: false
consequence: missense_variant
consequence: splice_region_variant
consequence: NMD_transcript_variant
ensembl gene: ENSG00000175274
ensembl protein: ENSP00000437243
ensembl transcript: ENST00000532253
gene symbol: TP53I11
hgvsc: ENST00000532253.1:c.131G>T
hgvsp: ENSP00000437243.1:p.Gly44Val
variant of: http://identifiers.org/hgnc/16842

GenotypeDepth
all individuals: 55
bin: 3.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 36329
bin: 2.5e0
variant carriers: 0

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

GenotypeDepth
all individuals: 911
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14371
bin: 7.5e0
variant carriers: 1

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

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2449
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 338
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1260
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 34396
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2534
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2216
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2653
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2762
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 235
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9505
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 9.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 588
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 334
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 78
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6102
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 1.189e1

DP
type: SiteQuality
SIO_000300: 3.02955e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.809999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

GenotypeDepth
all individuals: 340
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 832
bin: 1.25e1
variant carriers: 12

GenotypeDepth
all individuals: 21
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 114
bin: 1.75e1
variant carriers: 1

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

GenotypeDepth
all individuals: 37002
bin: 2.5e0
variant carriers: 20

GenotypeDepth
all individuals: 6
bin: 5.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 13301
bin: 7.5e0
variant carriers: 88

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

GenotypeDepth
all individuals: 1264
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 32
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 11
bin: 9.75e1
variant carriers: 10

GenotypeDepth
all individuals: 2446
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 111
bin: 9.75e1
variant carriers: 36

GenotypeQuality
all individuals: 2062
bin: 1.75e1
variant carriers: 12

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 642
bin: 6.75e1
variant carriers: 4

GenotypeQuality
all individuals: 217
bin: 7.25e1
variant carriers: 5

GenotypeQuality
all individuals: 2373
bin: 1.25e1
variant carriers: 7

GenotypeQuality
all individuals: 62
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 2.75e1
variant carriers: 6

GenotypeQuality
all individuals: 147
bin: 3.25e1
variant carriers: 6

GenotypeQuality
all individuals: 2784
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 48
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 8

GenotypeQuality
all individuals: 34788
bin: 7.5e0
variant carriers: 5

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 10

GenotypeQuality
all individuals: 131
bin: 8.25e1
variant carriers: 5

GenotypeQuality
all individuals: 242
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 2772
bin: 6.25e1
variant carriers: 8

GenotypeQuality
all individuals: 47
bin: 9.25e1
variant carriers: 5

GenotypeQuality
all individuals: 8728
bin: 2.25e1
variant carriers: 6

South Asian
type: Population
allele count: 6
allele frequency: 1.3215859030837e-2
allele num: 454
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 19
allele frequency: 3.093454900683816e-3
allele num: 6142
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.164556962025316e-3
allele num: 316
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.088307440719542e-4
allele num: 2446
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.68e-2

QD
type: SiteQuality
SIO_000300: 1.318e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.091e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

DP
type: SiteQuality
SIO_000300: 2.98682e5

VQSLOD
type: SiteQuality
SIO_000300: 2.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.22e-1

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

GenotypeDepth
all individuals: 2433
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 339
bin: 3.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 55
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 12950
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 1272
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1992
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2841
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2419
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8456
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35009
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 2.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 2746
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 642
bin: 6.75e1
variant carriers: 1

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.639344262295082e-4
allele num: 6100
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 3.225806451612903e-3
allele num: 310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 448
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.497e-1

DP
type: SiteQuality
SIO_000300: 2.96995e5

FS
type: SiteQuality
SIO_000300: 7.319e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.01e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.78e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 7.58e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 135
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 804
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1
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variant carriers: 0

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

GenotypeDepth
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African
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MQ
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BaseQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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InbreedingCoeff
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DP
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African
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East Asian
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VQSLOD
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MQRankSum
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DP
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InbreedingCoeff
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MQ
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ReadPosRankSum
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European (Finnish)
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Latino
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African
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East Asian
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South Asian
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European (Non-Finnish)
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ClippingRankSum
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FS
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QD
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DP
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VQSLOD
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MQ
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FS
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DP
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MQ
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FS
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MQ
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.083658430862592e-4
allele num: 9228
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8356
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5874
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60744
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 5.539e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.797e0

DP
type: SiteQuality
SIO_000300: 1.428081e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.377e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.486e0

QD
type: SiteQuality
SIO_000300: 2.45e1

GenotypeDepth
all individuals: 3884
bin: 3.25e1
variant carriers: 796

GenotypeDepth
all individuals: 8482
bin: 2.75e1
variant carriers: 1457

GenotypeDepth
all individuals: 511
bin: 4.75e1
variant carriers: 96

GenotypeDepth
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bin: 8.75e1
variant carriers: 29

GenotypeDepth
all individuals: 1215
bin: 9.75e1
variant carriers: 336

GenotypeDepth
all individuals: 146
bin: 9.25e1
variant carriers: 34

GenotypeDepth
all individuals: 10653
bin: 1.75e1
variant carriers: 1790

GenotypeDepth
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variant carriers: 28

GenotypeDepth
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bin: 3.75e1
variant carriers: 384

GenotypeDepth
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GenotypeDepth
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variant carriers: 995

GenotypeDepth
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variant carriers: 181

GenotypeDepth
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variant carriers: 22

GenotypeDepth
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variant carriers: 30

GenotypeDepth
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variant carriers: 41

GenotypeQuality
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bin: 7.75e1
variant carriers: 77

GenotypeQuality
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bin: 2.5e0
variant carriers: 10

GenotypeQuality
all individuals: 607
bin: 9.25e1
variant carriers: 67

GenotypeQuality
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bin: 4.75e1
variant carriers: 51

GenotypeQuality
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bin: 6.25e1
variant carriers: 62

GenotypeQuality
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variant carriers: 10

GenotypeQuality
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variant carriers: 30

GenotypeQuality
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GenotypeQuality
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variant carriers: 7829

GenotypeQuality
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variant carriers: 27

GenotypeQuality
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variant carriers: 17

GenotypeQuality
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variant carriers: 46

GenotypeQuality
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GenotypeQuality
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variant carriers: 20

GenotypeQuality
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variant carriers: 59

GenotypeQuality
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variant carriers: 62

GenotypeQuality
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variant carriers: 43

GenotypeQuality
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variant carriers: 62

GenotypeQuality
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variant carriers: 84

GenotypeQuality
all individuals: 2449
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variant carriers: 26

Other
type: Population
allele count: 62
allele frequency: 7.579462102689487e-2
allele num: 818
num of homozygotes: 4

African
type: Population
allele count: 833
allele frequency: 8.982100496010352e-2
allele num: 9274
num of homozygotes: 37

Latino
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allele count: 1696
allele frequency: 1.613087312155222e-1
allele num: 10514
num of homozygotes: 148

European (Finnish)
type: Population
allele count: 425
allele frequency: 7.257513661202186e-2
allele num: 5856
num of homozygotes: 8

European (Non-Finnish)
type: Population
allele count: 4196
allele frequency: 6.921579624558741e-2
allele num: 60622
num of homozygotes: 144

East Asian
type: Population
allele count: 142
allele frequency: 1.698158335326477e-2
allele num: 8362
num of homozygotes: 2

South Asian
type: Population
allele count: 1404
allele frequency: 9.194499017681729e-2
allele num: 15270
num of homozygotes: 75

BaseQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.76e0

MQ
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SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.98e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

QD
type: SiteQuality
SIO_000300: 1.603e1

DP
type: SiteQuality
SIO_000300: 1.465274e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.07e-1

GenotypeDepth
all individuals: 511
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1557
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variant carriers: 0

GenotypeDepth
all individuals: 792
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 4209
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GenotypeDepth
all individuals: 8482
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variant carriers: 0

GenotypeDepth
all individuals: 10653
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
all individuals: 386
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 198
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variant carriers: 0

GenotypeQuality
all individuals: 357
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variant carriers: 0

GenotypeQuality
all individuals: 606
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variant carriers: 0

GenotypeQuality
all individuals: 507
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1760
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variant carriers: 0

GenotypeQuality
all individuals: 1102
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.948698492296526e-5
allele num: 60622
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8362
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5856
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

DP
type: SiteQuality
SIO_000300: 1.465274e6

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.76e0

QD
type: SiteQuality
SIO_000300: 1.603e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.55e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.98e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.07e-1

GenotypeDepth
all individuals: 1029
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 410
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variant carriers: 0

GenotypeDepth
all individuals: 10593
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variant carriers: 1

GenotypeDepth
all individuals: 8871
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
all individuals: 4031
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variant carriers: 0

GenotypeDepth
all individuals: 4198
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GenotypeDepth
all individuals: 266
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GenotypeDepth
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GenotypeDepth
all individuals: 795
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GenotypeDepth
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GenotypeDepth
all individuals: 199
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GenotypeDepth
all individuals: 1542
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GenotypeDepth
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GenotypeQuality
all individuals: 5029
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 728
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variant carriers: 0

GenotypeQuality
all individuals: 600
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.277828766225252e-5
allele num: 61016
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10688
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.192748091603053e-4
allele num: 8384
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5912
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -9.93e-1

FS
type: SiteQuality
SIO_000300: 1.408e0

VQSLOD
type: SiteQuality
SIO_000300: 6.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 6.52e-1

DP
type: SiteQuality
SIO_000300: 1.462977e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.13e1

GenotypeDepth
all individuals: 19316
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variant carriers: 3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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
all individuals: 94
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 19991
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 12

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2293
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variant carriers: 0

GenotypeQuality
all individuals: 1854
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.89588093217573e-5
allele num: 61276
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 9.652509652509653e-4
allele num: 9324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8396
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5962
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10722
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

MQRankSum
type: SiteQuality
SIO_000300: -2.81e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.065e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

DP
type: SiteQuality
SIO_000300: 1.478966e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.62e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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
all individuals: 609
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 736
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GenotypeQuality
all individuals: 4794
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variant carriers: 0

GenotypeQuality
all individuals: 1844
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.915293115312777e-5
allele num: 61034
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.875117194824677e-4
allele num: 10666
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.1936022917164e-4
allele num: 8378
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9298
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15306
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.69434090138936e-4
allele num: 5902
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.43e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.29e-1

FS
type: SiteQuality
SIO_000300: 3.802e0

QD
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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African
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Latino
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Other
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East Asian
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European (Non-Finnish)
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allele frequency: 6.499626271489389e-5
allele num: 61542
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DP
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BaseQRankSum
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QD
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FS
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ClippingRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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African
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East Asian
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South Asian
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European (Finnish)
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FS
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DP
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ReadPosRankSum
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QD
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VQSLOD
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MQRankSum
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MQ
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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South Asian
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African
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Other
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European (Finnish)
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East Asian
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InbreedingCoeff
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MQ
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QD
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ClippingRankSum
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FS
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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Latino
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South Asian
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East Asian
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Other
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQRankSum
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FS
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BaseQRankSum
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VQSLOD
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MQ
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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South Asian
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East Asian
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Latino
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Other
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European (Non-Finnish)
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ReadPosRankSum
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DP
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VQSLOD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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QD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 20932

GenotypeQuality
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bin: 1.25e1
variant carriers: 82

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 436

European (Non-Finnish)
type: Population
allele count: 21821
allele frequency: 3.372955760967014e-1
allele num: 64694
num of homozygotes: 3525

East Asian
type: Population
allele count: 3
allele frequency: 3.519474425152511e-4
allele num: 8524
num of homozygotes: 0

Latino
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allele count: 1839
allele frequency: 1.662748643761302e-1
allele num: 11060
num of homozygotes: 144

South Asian
type: Population
allele count: 1842
allele frequency: 1.165970375996962e-1
allele num: 15798
num of homozygotes: 111

African
type: Population
allele count: 659
allele frequency: 6.936842105263158e-2
allele num: 9500
num of homozygotes: 24

Other
type: Population
allele count: 257
allele frequency: 2.954022988505747e-1
allele num: 870
num of homozygotes: 41

European (Finnish)
type: Population
allele count: 2544
allele frequency: 3.996229971724788e-1
allele num: 6366
num of homozygotes: 489

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

QD
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SIO_000300: 1.5e1

VQSLOD
type: SiteQuality
SIO_000300: 5.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

DP
type: SiteQuality
SIO_000300: 1.825705e6

FS
type: SiteQuality
SIO_000300: 6.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.143e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.06e-2

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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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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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: 671
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variant carriers: 0

Latino
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allele count: 3
allele frequency: 2.69493352497305e-4
allele num: 11132
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15798
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533836431682925e-5
allele num: 65196
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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SIO_000300: -9.5e-2

VQSLOD
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SIO_000300: 1.07e0

ClippingRankSum
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SIO_000300: -6.24e-1

DP
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SIO_000300: 1.651481e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.056e1

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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 681
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11222
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15930
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.042752867570386e-4
allele num: 9590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65526
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.163e1

MQ
type: SiteQuality
SIO_000300: 3.7e1

FS
type: SiteQuality
SIO_000300: 1.1171e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.535e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

DP
type: SiteQuality
SIO_000300: 1.669832e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.83e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.16e0

MQRankSum
type: SiteQuality
SIO_000300: -8.599999999999999e-2

ReadPosRankSum
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SIO_000300: 1.85e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 611
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11226
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.578754578754579e-5
allele num: 65520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15940
num of homozygotes: 0

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: -5.8e-1

FS
type: SiteQuality
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ClippingRankSum
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SIO_000300: -3.26e-1

InbreedingCoeff
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DP
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ReadPosRankSum
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SIO_000300: 6.42e-1

BaseQRankSum
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SIO_000300: -2.59e0

MQ
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SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 6.61e-1

QD
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SIO_000300: 1.214e1

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.037129226301597e-4
allele num: 9642
num of homozygotes: 0

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

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

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

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 35881
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GenotypeQuality
all individuals: 416
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9660
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.2465719272002e-4
allele num: 16044
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11294
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.520820026158105e-4
allele num: 65754
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.689641e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

QD
type: SiteQuality
SIO_000300: 1.285e1

GenotypeDepth
all individuals: 245
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2384
bin: 3.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 3.25e1
variant carriers: 0

GenotypeDepth
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bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 300
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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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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 436
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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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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 199
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 272
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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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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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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 2341
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518787400139728e-5
allele num: 65842
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9698
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16068
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.862e1

QD
type: SiteQuality
SIO_000300: 7.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.862e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.419999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.697018e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.244e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e-1

GenotypeDepth
all individuals: 1395
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 77
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variant carriers: 0

GenotypeDepth
all individuals: 19356
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variant carriers: 0

GenotypeDepth
all individuals: 436
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 2393
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variant carriers: 0

GenotypeDepth
all individuals: 759
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 245
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variant carriers: 0

GenotypeDepth
all individuals: 300
bin: 6.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 324
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variant carriers: 0

GenotypeDepth
all individuals: 1218
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 593
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 199
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variant carriers: 0

GenotypeDepth
all individuals: 156
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variant carriers: 0

GenotypeDepth
all individuals: 573
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 423
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variant carriers: 0

GenotypeQuality
all individuals: 7788
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variant carriers: 0

GenotypeQuality
all individuals: 148
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variant carriers: 0

GenotypeQuality
all individuals: 2334
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1825
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 255
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 4405
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2581
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variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9694
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16070
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.037574800279457e-5
allele num: 65842
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.33e-1

DP
type: SiteQuality
SIO_000300: 1.69792e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.91e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.8e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.56e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.908e0

QD
type: SiteQuality
SIO_000300: 8.359999999999999e0

GenotypeDepth
all individuals: 300
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 77
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variant carriers: 0

GenotypeDepth
all individuals: 156
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variant carriers: 0

GenotypeDepth
all individuals: 23328
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 607
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variant carriers: 0

GenotypeDepth
all individuals: 245
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variant carriers: 0

GenotypeDepth
all individuals: 1188
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 572
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 400
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 17
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variant carriers: 0

GenotypeDepth
all individuals: 1437
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7501
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 436
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 114
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variant carriers: 0

GenotypeDepth
all individuals: 19434
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variant carriers: 0

GenotypeDepth
all individuals: 1229
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variant carriers: 0

GenotypeDepth
all individuals: 758
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7759
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1899
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variant carriers: 0

GenotypeQuality
all individuals: 2334
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4404
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1541
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11312
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.222775357809582e-5
allele num: 16070
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9714
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.518879674352198e-5
allele num: 65838
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.448e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.292e0

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 4.87e0

DP
type: SiteQuality
SIO_000300: 1.69773e6

GenotypeDepth
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bin: 7.25e1
variant carriers: 0

GenotypeDepth
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bin: 8.25e1
variant carriers: 1

GenotypeDepth
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bin: 1.75e1
variant carriers: 0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
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bin: 7.5e0
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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bin: 2.75e1
variant carriers: 0

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
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bin: 3.25e1
variant carriers: 0

GenotypeDepth
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bin: 6.75e1
variant carriers: 0

GenotypeDepth
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bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 572
bin: 5.25e1
variant carriers: 0

GenotypeDepth
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bin: 2.25e1
variant carriers: 0

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 1189
bin: 4.25e1
variant carriers: 0

GenotypeDepth
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bin: 5.75e1
variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 276
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2316
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7682
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36174
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16052
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.031140441328109e-4
allele num: 9698
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65706
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11292
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.399e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.11e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

QD
type: SiteQuality
SIO_000300: 9.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 3.026e0

VQSLOD
type: SiteQuality
SIO_000300: 5.93e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.5e-1

DP
type: SiteQuality
SIO_000300: 1.691118e6

Annotation
canonical: false
consequence: synonymous_variant
consequence: splice_region_variant
ensembl gene: ENSG00000175274
ensembl protein: ENSP00000431556
ensembl transcript: ENST00000527685
gene symbol: TP53I11
hgvsc: ENST00000527685.1:c.132C>A
hgvsp: ENST00000527685.1:c.132C>A(p.%3D)
variant of: http://identifiers.org/hgnc/16842

GenotypeDepth
all individuals: 437
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1196
bin: 4.25e1
variant carriers: 8

GenotypeDepth
all individuals: 41
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 19277
bin: 2.75e1
variant carriers: 6

GenotypeDepth
all individuals: 808
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2243
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 246
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 300
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 200
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 7456
bin: 3.25e1
variant carriers: 8

GenotypeDepth
all individuals: 115
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 157
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1353
bin: 7.5e0
variant carriers: 0

GenotypeDepth
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bin: 2.25e1
variant carriers: 3

GenotypeDepth
all individuals: 2379
bin: 3.75e1
variant carriers: 3

GenotypeDepth
all individuals: 326
bin: 6.25e1
variant carriers: 2

GenotypeDepth
all individuals: 407
bin: 5.75e1
variant carriers: 8

GenotypeDepth
all individuals: 575
bin: 5.25e1
variant carriers: 3

GenotypeDepth
all individuals: 78
bin: 9.25e1
variant carriers: 2

GenotypeDepth
all individuals: 761
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 595
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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East Asian
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European (Finnish)
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African
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European (Non-Finnish)
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InbreedingCoeff
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DP
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VQSLOD
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MQ
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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QD
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FS
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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South Asian
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European (Finnish)
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African
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Other
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European (Non-Finnish)
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East Asian
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FS
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQRankSum
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ClippingRankSum
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DP
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MQ
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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South Asian
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BaseQRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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MQ
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FS
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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South Asian
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MQRankSum
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VQSLOD
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QD
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DP
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ReadPosRankSum
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MQ
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FS
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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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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Latino
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European (Finnish)
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FS
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DP
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ClippingRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2223
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9558
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65030
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.280618012812461e-5
allele num: 15922
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11158
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6352
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

QD
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -1.3e-3

MQ
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SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.36e-1

FS
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.570226e6

VQSLOD
type: SiteQuality
SIO_000300: -2.034e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.93e0

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

Other
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allele count: 0
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num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.165772907437631e-4
allele num: 8578
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15800
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64578
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6294
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.81e-1

VQSLOD
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SIO_000300: -1.342e0

DP
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SIO_000300: 1.524158e6

FS
type: SiteQuality
SIO_000300: 2.092e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.26e-1

MQRankSum
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SIO_000300: -1.919e0

MQ
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SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.6e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

GenotypeDepth
all individuals: 192
bin: 2.5e0
variant carriers: 9

GenotypeDepth
all individuals: 6936
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variant carriers: 636

GenotypeDepth
all individuals: 2052
bin: 7.5e0
variant carriers: 165

GenotypeDepth
all individuals: 452
bin: 9.75e1
variant carriers: 107

GenotypeDepth
all individuals: 619
bin: 5.25e1
variant carriers: 134

GenotypeDepth
all individuals: 11256
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variant carriers: 1633

GenotypeDepth
all individuals: 304
bin: 6.75e1
variant carriers: 52

GenotypeDepth
all individuals: 407
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variant carriers: 84

GenotypeDepth
all individuals: 14529
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variant carriers: 1772

GenotypeDepth
all individuals: 248
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variant carriers: 46

GenotypeDepth
all individuals: 2512
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variant carriers: 695

GenotypeDepth
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variant carriers: 39

GenotypeDepth
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variant carriers: 18

GenotypeDepth
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variant carriers: 243

GenotypeDepth
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variant carriers: 59

GenotypeDepth
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variant carriers: 30

GenotypeDepth
all individuals: 123
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variant carriers: 30

GenotypeQuality
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variant carriers: 55

GenotypeQuality
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variant carriers: 18

GenotypeQuality
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bin: 7.25e1
variant carriers: 38

GenotypeQuality
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variant carriers: 25

GenotypeQuality
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bin: 1.75e1
variant carriers: 23

GenotypeQuality
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variant carriers: 11

GenotypeQuality
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variant carriers: 51

GenotypeQuality
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variant carriers: 8074

GenotypeQuality
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GenotypeQuality
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variant carriers: 20

GenotypeQuality
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variant carriers: 11

GenotypeQuality
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variant carriers: 24

GenotypeQuality
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variant carriers: 36

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 33

GenotypeQuality
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variant carriers: 59

GenotypeQuality
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variant carriers: 60

GenotypeQuality
all individuals: 387
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variant carriers: 9

GenotypeQuality
all individuals: 12343
bin: 6.25e1
variant carriers: 45

Latino
type: Population
allele count: 1711
allele frequency: 1.557720320466132e-1
allele num: 10984
num of homozygotes: 149

Other
type: Population
allele count: 68
allele frequency: 7.981220657276995e-2
allele num: 852
num of homozygotes: 5

European (Non-Finnish)
type: Population
allele count: 4276
allele frequency: 6.66271931191374e-2
allele num: 64178
num of homozygotes: 146

African
type: Population
allele count: 845
allele frequency: 8.932346723044397e-2
allele num: 9460
num of homozygotes: 41

East Asian
type: Population
allele count: 148
allele frequency: 1.728971962616822e-2
allele num: 8560
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 434
allele frequency: 6.96405648267009e-2
allele num: 6232
num of homozygotes: 11

South Asian
type: Population
allele count: 1423
allele frequency: 9.026896726719107e-2
allele num: 15764
num of homozygotes: 77

VQSLOD
type: SiteQuality
SIO_000300: 5.94e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.52609e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.3e-2

QD
type: SiteQuality
SIO_000300: 1.479e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.57e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 12195
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2512
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 14529
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 5916
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variant carriers: 0

GenotypeDepth
all individuals: 407
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GenotypeDepth
all individuals: 123
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GenotypeDepth
all individuals: 192
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GenotypeDepth
all individuals: 2052
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1383
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GenotypeQuality
all individuals: 620
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15764
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.116332699679018e-5
allele num: 64178
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10984
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9460
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.94e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-2

FS
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BaseQRankSum
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DP
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SIO_000300: 1.52609e6

MQRankSum
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SIO_000300: 5.3e-2

ClippingRankSum
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.9e-2

QD
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SIO_000300: 1.479e1

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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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
all individuals: 1338
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GenotypeQuality
all individuals: 3011
bin: 2.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10920
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.628664495114007e-4
allele num: 6140
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.93e-1

BaseQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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MQ
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MQRankSum
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VQSLOD
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DP
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SIO_000300: 1.484819e6

QD
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SIO_000300: 1.05e0

GenotypeDepth
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variant carriers: 85

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 607

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2143
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variant carriers: 1264

GenotypeQuality
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variant carriers: 1177

GenotypeQuality
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GenotypeQuality
all individuals: 2801
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GenotypeQuality
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variant carriers: 1202

GenotypeQuality
all individuals: 1341
bin: 5.75e1
variant carriers: 670

GenotypeQuality
all individuals: 1343
bin: 8.25e1
variant carriers: 1026

East Asian
type: Population
allele count: 5689
allele frequency: 6.785543893129771e-1
allele num: 8384
num of homozygotes: 1926

European (Non-Finnish)
type: Population
allele count: 26735
allele frequency: 4.288166041125333e-1
allele num: 62346
num of homozygotes: 5549

African
type: Population
allele count: 2906
allele frequency: 3.134167385677308e-1
allele num: 9272
num of homozygotes: 438

Latino
type: Population
allele count: 5257
allele frequency: 4.946368084305608e-1
allele num: 10628
num of homozygotes: 1257

South Asian
type: Population
allele count: 9815
allele frequency: 6.250796076932875e-1
allele num: 15702
num of homozygotes: 3107

Other
type: Population
allele count: 393
allele frequency: 4.723557692307692e-1
allele num: 832
num of homozygotes: 100

European (Finnish)
type: Population
allele count: 2685
allele frequency: 4.458651610760545e-1
allele num: 6022
num of homozygotes: 571

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.66e0

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-2

DP
type: SiteQuality
SIO_000300: 1.50167e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.088e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.03e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.24e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.19e-1

GenotypeDepth
all individuals: 4920
bin: 3.25e1
variant carriers: 1

GenotypeDepth
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bin: 1.75e1
variant carriers: 0

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

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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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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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 640
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62820
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6058
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10752
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.08201687946332e-4
allele num: 9242
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15550
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8416
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.694e0

MQRankSum
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SIO_000300: 4.11e-1

FS
type: SiteQuality
SIO_000300: 1.1957e1

DP
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SIO_000300: 1.455056e6

VQSLOD
type: SiteQuality
SIO_000300: -1.895e0

QD
type: SiteQuality
SIO_000300: 2.965e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 20075
bin: 1.25e1
variant carriers: 8

GenotypeDepth
all individuals: 10498
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variant carriers: 1

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeDepth
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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: 5

GenotypeDepth
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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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variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 2

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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GenotypeQuality
all individuals: 225
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GenotypeQuality
all individuals: 831
bin: 9.75e1
variant carriers: 19

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7166
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11642
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9358
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.903657727290471e-5
allele num: 51234
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 16
allele frequency: 4.459308807134894e-3
allele num: 3588
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.315e0

QD
type: SiteQuality
SIO_000300: 1.163e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

DP
type: SiteQuality
SIO_000300: 8.97741e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 256
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 31
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variant carriers: 0

GenotypeDepth
all individuals: 11
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variant carriers: 0

GenotypeDepth
all individuals: 2010
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variant carriers: 0

GenotypeDepth
all individuals: 12381
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variant carriers: 2

GenotypeDepth
all individuals: 12124
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
all individuals: 7
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variant carriers: 0

GenotypeDepth
all individuals: 63
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variant carriers: 0

GenotypeDepth
all individuals: 19689
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variant carriers: 3

GenotypeDepth
all individuals: 9801
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variant carriers: 3

GenotypeDepth
all individuals: 343
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GenotypeDepth
all individuals: 17
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GenotypeDepth
all individuals: 214
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GenotypeDepth
all individuals: 121
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GenotypeDepth
all individuals: 6
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GenotypeDepth
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GenotypeQuality
all individuals: 1273
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7192
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.774840615767377e-5
allele num: 51448
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11592
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3624
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 4.264392324093816e-4
allele num: 9380
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -5.15e-1

BaseQRankSum
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SIO_000300: -9.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.16e-1

FS
type: SiteQuality
SIO_000300: 1.311e0

DP
type: SiteQuality
SIO_000300: 9.13444e5

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.12e-1

QD
type: SiteQuality
SIO_000300: 1.244e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9482
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3672
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11790
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.929235636840684e-5
allele num: 51834
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7246
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.06e-1

MQRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: -4.9e-3

FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 9.47314e5

QD
type: SiteQuality
SIO_000300: 9.859999999999999e0

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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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
all individuals: 3749
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variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.34698275862069e-4
allele num: 7424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52962
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12038
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7786
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9652
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3820
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e0

DP
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MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 7.76e-1

FS
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VQSLOD
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BaseQRankSum
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QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

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