5-65310601-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65310601
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65310601
    reference: chr 5
allele count: 1
allele frequency: 2.026424576477264e-5
allele num: 49348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.533+48T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.533+48T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.533+48T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.533+48T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.533+48T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.533+48T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.533+48T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.533+48T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.533+48T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.533+48T>A
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5949
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2720
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12777
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

5-65310601-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65310601
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65310601
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 49348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.533+48T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.533+48T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.533+48T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.533+48T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.533+48T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.533+48T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.533+48T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.533+48T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.533+48T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.533+48T>G
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5949
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12264
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12777
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3641
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1682
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1178
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

5-65310604-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65310604
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65310604
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 45568
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.533+51T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.533+51T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.533+51T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.533+51T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.533+51T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.533+51T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.533+51T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.533+51T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.533+51T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.533+51T>C
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5859
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18758
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13062
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2708
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1260
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 9.25e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

5-65310605-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65310605
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65310605
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 45810
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.533+52T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.533+52T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.533+52T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.533+52T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.533+52T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.533+52T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.533+52T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.533+52T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.533+52T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.533+52T>A
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 13105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5852
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12273
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18730
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 965
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8518
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4476
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5027
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

5-65317105-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317105
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317105
    reference: chr 5
allele count: 91
allele frequency: 8.308529481584282e-4
allele num: 109526
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.534-45A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.534-45A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.534-45A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.534-45A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.534-45A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.534-45A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.534-45A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.534-45A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.534-45A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.534-45A>G
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13354
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 2.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 12187
  bin: 1.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5067
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11426
  bin: 2.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1476
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2370
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5764
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6036
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 3
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

5-65317108-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317108
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317108
    reference: chr 5
allele count: 3
allele frequency: 2.741829348541347e-5
allele num: 109416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.534-42G>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.534-42G>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.534-42G>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.534-42G>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.534-42G>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.534-42G>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.534-42G>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.534-42G>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.534-42G>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.534-42G>T
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10110
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12985
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13612
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5037
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5957
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9871
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1253
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

5-65317111-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317111
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317111
    reference: chr 5
allele count: 9
allele frequency: 8.191648159609713e-5
allele num: 109868
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.534-39A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.534-39A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.534-39A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.534-39A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.534-39A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.534-39A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.534-39A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.534-39A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.534-39A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.534-39A>G
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16049
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8113
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5026
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12381
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1475
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 889
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2243
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

5-65317119-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317119
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317119
    reference: chr 5
allele count: 1
allele frequency: 9.040610422015694e-6
allele num: 110612
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.534-31A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.534-31A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.534-31A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.534-31A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.534-31A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.534-31A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.534-31A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.534-31A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.534-31A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.534-31A>G
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4784
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9780
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1184
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 845
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum

5-65317134-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317134
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317134
    reference: chr 5
allele count: 1
allele frequency: 8.722502311463112e-6
allele num: 114646
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.534-16A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.534-16A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.534-16A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.534-16A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.534-16A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.534-16A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.534-16A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.534-16A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.534-16A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.534-16A>G
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31216
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3223
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4653
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1472
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

5-65317154-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317154
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317154
    reference: chr 5
allele count: 1
allele frequency: 8.456945689494782e-6
allele num: 118246
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.538A>G
  hgvsp: ENSP00000284037.4:p.Met180Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.538A>G
  hgvsp: ENSP00000422766.1:p.Met180Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.538A>G
  hgvsp: ENSP00000422015.1:p.Met180Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.538A>G
  hgvsp: ENSP00000370330.2:p.Met180Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.538A>G
  hgvsp: ENSP00000370326.2:p.Met180Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.538A>G
  hgvsp: ENSP00000426632.1:p.Met180Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.538A>G
  hgvsp: ENSP00000397833.2:p.Met180Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.538A>G
  hgvsp: ENSP00000370323.1:p.Met180Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.538A>G
  hgvsp: ENSP00000370325.2:p.Met180Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.538A>G
  hgvsp: ENSP00000370322.1:p.Met180Val
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8585
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1515
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1427
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3961
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Met180Val
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

5-65317158-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317158
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317158
    reference: chr 5
allele count: 74
allele frequency: 6.239565591325318e-4
allele num: 118598
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.542A>G
  hgvsp: ENSP00000370323.1:p.Asn181Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.542A>G
  hgvsp: ENSP00000370325.2:p.Asn181Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.542A>G
  hgvsp: ENSP00000422766.1:p.Asn181Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.542A>G
  hgvsp: ENSP00000422015.1:p.Asn181Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.542A>G
  hgvsp: ENSP00000370326.2:p.Asn181Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.542A>G
  hgvsp: ENSP00000397833.2:p.Asn181Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.542A>G
  hgvsp: ENSP00000370322.1:p.Asn181Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.542A>G
  hgvsp: ENSP00000284037.4:p.Asn181Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.542A>G
  hgvsp: ENSP00000370330.2:p.Asn181Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.542A>G
  hgvsp: ENSP00000426632.1:p.Asn181Ser
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 34007
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4049
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8748
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn181Ser
num of homozygotes: 2
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

5-65317166-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317166
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317166
    reference: chr 5
allele count: 1
allele frequency: 8.395177809866013e-6
allele num: 119116
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.550A>T
  hgvsp: ENSP00000370323.1:p.Thr184Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.550A>T
  hgvsp: ENSP00000422015.1:p.Thr184Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.550A>T
  hgvsp: ENSP00000370325.2:p.Thr184Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.550A>T
  hgvsp: ENSP00000284037.4:p.Thr184Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.550A>T
  hgvsp: ENSP00000370330.2:p.Thr184Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.550A>T
  hgvsp: ENSP00000397833.2:p.Thr184Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.550A>T
  hgvsp: ENSP00000370322.1:p.Thr184Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.550A>T
  hgvsp: ENSP00000370326.2:p.Thr184Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.550A>T
  hgvsp: ENSP00000422766.1:p.Thr184Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.550A>T
  hgvsp: ENSP00000426632.1:p.Thr184Ser
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1086
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr184Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD

5-65317176-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317176
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317176
    reference: chr 5
allele count: 1
allele frequency: 8.361343835181191e-6
allele num: 119598
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.560A>G
  hgvsp: ENSP00000397833.2:p.Glu187Gly
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.560A>G
  hgvsp: ENSP00000370325.2:p.Glu187Gly
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.560A>G
  hgvsp: ENSP00000370330.2:p.Glu187Gly
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.560A>G
  hgvsp: ENSP00000370322.1:p.Glu187Gly
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.560A>G
  hgvsp: ENSP00000284037.4:p.Glu187Gly
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.560A>G
  hgvsp: ENSP00000422766.1:p.Glu187Gly
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.560A>G
  hgvsp: ENSP00000422015.1:p.Glu187Gly
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.560A>G
  hgvsp: ENSP00000370326.2:p.Glu187Gly
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.560A>G
  hgvsp: ENSP00000370323.1:p.Glu187Gly
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.560A>G
  hgvsp: ENSP00000426632.1:p.Glu187Gly
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9487
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1991
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu187Gly
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

5-65317181-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317181
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317181
    reference: chr 5
allele count: 93249
allele frequency: 7.707548105534616e-1
allele num: 120984
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.565C>T
  hgvsp: ENST00000380943.2:c.565C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.565C>T
  hgvsp: ENST00000511297.1:c.565C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.565C>T
  hgvsp: ENST00000416865.2:c.565C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.565C>T
  hgvsp: ENST00000380936.1:c.565C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.565C>T
  hgvsp: ENST00000380939.2:c.565C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.565C>T
  hgvsp: ENST00000380938.2:c.565C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.565C>T
  hgvsp: ENST00000506030.1:c.565C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.565C>T
  hgvsp: ENST00000284037.5:c.565C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.565C>T
  hgvsp: ENST00000380935.1:c.565C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.565C>T
  hgvsp: ENST00000508515.1:c.565C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6109
  bin: 3.75e1
  variant carriers: 5975
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 6.75e1
  variant carriers: 2505
genotype depth: GenotypeDepth
  all individuals: 6218
  bin: 4.25e1
  variant carriers: 6126
genotype depth: GenotypeDepth
  all individuals: 1008
  bin: 1.75e1
  variant carriers: 1001
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.25e1
  variant carriers: 301
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 5070
  bin: 2.75e1
  variant carriers: 3979
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5808
  bin: 3.25e1
  variant carriers: 5480
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 5.75e1
  variant carriers: 3830
genotype depth: GenotypeDepth
  all individuals: 4841
  bin: 5.25e1
  variant carriers: 4797
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 2.25e1
  variant carriers: 2238
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 6.25e1
  variant carriers: 3142
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 8.25e1
  variant carriers: 1240
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 8.75e1
  variant carriers: 1040
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 9.25e1
  variant carriers: 780
genotype depth: GenotypeDepth
  all individuals: 5608
  bin: 4.75e1
  variant carriers: 5525
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 7.25e1
  variant carriers: 1952
genotype depth: GenotypeDepth
  all individuals: 4536
  bin: 9.75e1
  variant carriers: 4476
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 7.75e1
  variant carriers: 1619
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 5.75e1
  variant carriers: 285
hgvs: p.Leu189Leu
num of homozygotes: 37313
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

5-65317189-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317189
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317189
    reference: chr 5
allele count: 1
allele frequency: 8.335139280177371e-6
allele num: 119974
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.573G>A
  hgvsp: ENST00000506030.1:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.573G>A
  hgvsp: ENST00000416865.2:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.573G>A
  hgvsp: ENST00000380936.1:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.573G>A
  hgvsp: ENST00000284037.5:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.573G>A
  hgvsp: ENST00000380943.2:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.573G>A
  hgvsp: ENST00000380938.2:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.573G>A
  hgvsp: ENST00000511297.1:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.573G>A
  hgvsp: ENST00000380939.2:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.573G>A
  hgvsp: ENST00000508515.1:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.573G>A
  hgvsp: ENST00000380935.1:c.573G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27549
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10616
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12745
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu191Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

5-65317190-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317190
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317190
    reference: chr 5
allele count: 1
allele frequency: 8.333750020834376e-6
allele num: 119994
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.574G>C
  hgvsp: ENSP00000422766.1:p.Gly192Arg
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.574G>C
  hgvsp: ENSP00000284037.4:p.Gly192Arg
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.574G>C
  hgvsp: ENSP00000422015.1:p.Gly192Arg
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.574G>C
  hgvsp: ENSP00000370322.1:p.Gly192Arg
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.574G>C
  hgvsp: ENSP00000370326.2:p.Gly192Arg
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.574G>C
  hgvsp: ENSP00000370323.1:p.Gly192Arg
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.574G>C
  hgvsp: ENSP00000370325.2:p.Gly192Arg
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.574G>C
  hgvsp: ENSP00000397833.2:p.Gly192Arg
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.574G>C
  hgvsp: ENSP00000370330.2:p.Gly192Arg
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.574G>C
  hgvsp: ENSP00000426632.1:p.Gly192Arg
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2493
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly192Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ

5-65317194-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317194
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317194
    reference: chr 5
allele count: 4
allele frequency: 3.338730948366526e-5
allele num: 119806
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.578G>A
  hgvsp: ENSP00000422766.1:p.Ser193Asn
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.578G>A
  hgvsp: ENSP00000370323.1:p.Ser193Asn
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.578G>A
  hgvsp: ENSP00000370325.2:p.Ser193Asn
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.578G>A
  hgvsp: ENSP00000370330.2:p.Ser193Asn
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.578G>A
  hgvsp: ENSP00000422015.1:p.Ser193Asn
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.578G>A
  hgvsp: ENSP00000397833.2:p.Ser193Asn
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.578G>A
  hgvsp: ENSP00000284037.4:p.Ser193Asn
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.578G>A
  hgvsp: ENSP00000426632.1:p.Ser193Asn
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.578G>A
  hgvsp: ENSP00000370326.2:p.Ser193Asn
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.578G>A
  hgvsp: ENSP00000370322.1:p.Ser193Asn
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12742
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10514
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2481
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser193Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

5-65317199-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317199
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317199
    reference: chr 5
allele count: 1
allele frequency: 8.380403265005112e-6
allele num: 119326
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.583G>A
  hgvsp: ENSP00000397833.2:p.Glu195Lys
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.583G>A
  hgvsp: ENSP00000370325.2:p.Glu195Lys
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.583G>A
  hgvsp: ENSP00000284037.4:p.Glu195Lys
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.583G>A
  hgvsp: ENSP00000370330.2:p.Glu195Lys
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.583G>A
  hgvsp: ENSP00000422766.1:p.Glu195Lys
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.583G>A
  hgvsp: ENSP00000426632.1:p.Glu195Lys
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.583G>A
  hgvsp: ENSP00000370323.1:p.Glu195Lys
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.583G>A
  hgvsp: ENSP00000370326.2:p.Glu195Lys
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.583G>A
  hgvsp: ENSP00000370322.1:p.Glu195Lys
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.583G>A
  hgvsp: ENSP00000422015.1:p.Glu195Lys
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27105
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10404
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu195Lys
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

5-65317206-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317206
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317206
    reference: chr 5
allele count: 82
allele frequency: 6.896435720172916e-4
allele num: 118902
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.590C>T
  hgvsp: ENSP00000370325.2:p.Thr197Met
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.590C>T
  hgvsp: ENSP00000370322.1:p.Thr197Met
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.590C>T
  hgvsp: ENSP00000422015.1:p.Thr197Met
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.590C>T
  hgvsp: ENSP00000397833.2:p.Thr197Met
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.590C>T
  hgvsp: ENSP00000370323.1:p.Thr197Met
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.590C>T
  hgvsp: ENSP00000370330.2:p.Thr197Met
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.590C>T
  hgvsp: ENSP00000284037.4:p.Thr197Met
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.590C>T
  hgvsp: ENSP00000422766.1:p.Thr197Met
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.590C>T
  hgvsp: ENSP00000370326.2:p.Thr197Met
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.590C>T
  hgvsp: ENSP00000426632.1:p.Thr197Met
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26647
  bin: 2.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10216
  bin: 3.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12211
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1116
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7613
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr197Met
num of homozygotes: 1
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

5-65317207-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317207
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317207
    reference: chr 5
allele count: 3
allele frequency: 2.525805310926634e-5
allele num: 118774
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.591G>A
  hgvsp: ENST00000380939.2:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.591G>A
  hgvsp: ENST00000284037.5:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.591G>A
  hgvsp: ENST00000506030.1:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.591G>A
  hgvsp: ENST00000380935.1:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.591G>A
  hgvsp: ENST00000380943.2:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.591G>A
  hgvsp: ENST00000511297.1:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.591G>A
  hgvsp: ENST00000380936.1:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.591G>A
  hgvsp: ENST00000416865.2:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.591G>A
  hgvsp: ENST00000508515.1:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.591G>A
  hgvsp: ENST00000380938.2:c.591G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1789
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr197Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD

5-65317226-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317226
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317226
    reference: chr 5
allele count: 1
allele frequency: 8.566337719298245e-6
allele num: 116736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.597+13C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.597+13C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.597+13C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.597+13C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.597+13C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.597+13C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.597+13C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.597+13C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.597+13C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.597+13C>T
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1529
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11166
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5921
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23394
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 627
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
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: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

5-65317234-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317234
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317234
    reference: chr 5
allele count: 1
allele frequency: 8.659808098652533e-6
allele num: 115476
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.597+21C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.597+21C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.597+21C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.597+21C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.597+21C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.597+21C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.597+21C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.597+21C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.597+21C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.597+21C>G
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2809
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20629
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9658
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2670
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9356
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1375
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4594
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2612
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum

5-65317238-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317238
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317238
    reference: chr 5
allele count: 3
allele frequency: 2.610284521012791e-5
allele num: 114930
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.597+25C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.597+25C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.597+25C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.597+25C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.597+25C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.597+25C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.597+25C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.597+25C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.597+25C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.597+25C>T
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3987
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18859
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8570
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1207
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

5-65317246-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317246
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317246
    reference: chr 5
allele count: 1
allele frequency: 8.785030308354564e-6
allele num: 113830
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.597+33T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.597+33T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.597+33T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.597+33T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.597+33T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.597+33T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.597+33T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.597+33T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.597+33T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.597+33T>C
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6846
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14998
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5902
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

5-65317247-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317247
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317247
    reference: chr 5
allele count: 1
allele frequency: 8.814300320840532e-6
allele num: 113452
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.597+34C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.597+34C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.597+34C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.597+34C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.597+34C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.597+34C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.597+34C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.597+34C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.597+34C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.597+34C>T
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1856
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13659
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9046
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15193
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5963
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3968
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

5-65317249-T-TCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317249
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317251
    reference: chr 5
allele count: 1
allele frequency: 8.845017601585028e-6
allele num: 113058
alternate allele: TCC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.597+36_597+37insCC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.597+36_597+37insCC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.597+36_597+37insCC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.597+36_597+37insCC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.597+36_597+37insCC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.597+36_597+37insCC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.597+36_597+37insCC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.597+36_597+37insCC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.597+36_597+37insCC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.597+36_597+37insCC
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 12444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10578
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15434
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1820
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6174
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4582
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/5-65317250-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317250
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317250
    reference: chr 5
allele count: 1
allele frequency: 8.880994671403197e-6
allele num: 112600
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.597+37A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.597+37A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.597+37A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.597+37A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.597+37A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.597+37A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.597+37A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.597+37A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.597+37A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.597+37A>C
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3598
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12540
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15391
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4996
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14649
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6999
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

5-65317251-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317251
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317251
    reference: chr 5
allele count: 2
allele frequency: 1.777398599409904e-5
allele num: 112524
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.597+38T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.597+38T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.597+38T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.597+38T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.597+38T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.597+38T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.597+38T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.597+38T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.597+38T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.597+38T>C
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3612
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12544
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 833
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4183
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11321
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

5-65317251-TATTTAATG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317251
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317243
    reference: chr 5
allele count: 1
allele frequency: 8.886992997049519e-6
allele num: 112524
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3612
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5812
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12544
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15393
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4183
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 860
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 833
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: TATTTAATG
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS

5-65317255-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317255
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317255
    reference: chr 5
allele count: 5
allele frequency: 4.505235083166639e-5
allele num: 110982
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.597+42T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.597+42T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.597+42T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.597+42T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.597+42T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.597+42T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.597+42T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.597+42T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.597+42T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.597+42T>A
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14931
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15409
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4255
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6063
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10698
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 593
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

5-65317262-GAACAAAATATGAAAATTAATGTA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65317262
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65317239
    reference: chr 5
allele count: 1
allele frequency: 9.369261327436946e-6
allele num: 106732
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5647
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15000
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10013
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14021
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2946
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4580
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5206
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4243
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
reference allele: GAACAAAATATGAAAATTAATGTA
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

5-65319067-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319067
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319067
    reference: chr 5
allele count: 1
allele frequency: 8.254639107178234e-6
allele num: 121144
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.598-51A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.598-51A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.598-51A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.598-51A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.368A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.598-51A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.598-51A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.598-51A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.598-51A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.598-51A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.598-51A>T
  variant of: http://identifiers.org/hgnc/15842
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9509
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

5-65319068-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319068
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319068
    reference: chr 5
allele count: 1
allele frequency: 8.256138438929344e-6
allele num: 121122
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.598-50T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.598-50T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.598-50T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.598-50T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.598-50T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.598-50T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.598-50T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.369T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.598-50T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.598-50T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.598-50T>G
  variant of: http://identifiers.org/hgnc/15842
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9507
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11074
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1339
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8873
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2947
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

5-65319075-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319075
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319075
    reference: chr 5
allele count: 1
allele frequency: 8.25218682950982e-6
allele num: 121180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.598-43A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.598-43A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.598-43A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.598-43A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.376A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.598-43A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.598-43A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.598-43A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.598-43A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.598-43A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.598-43A>G
  variant of: http://identifiers.org/hgnc/15842
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7423
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

5-65319081-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319081
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319081
    reference: chr 5
allele count: 1
allele frequency: 8.250688932525866e-6
allele num: 121202
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.382A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.598-37A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.598-37A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.598-37A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.598-37A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.598-37A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.598-37A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.598-37A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.598-37A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.598-37A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.598-37A>G
  variant of: http://identifiers.org/hgnc/15842
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7424
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ

http://identifiers.org/exac.variant/5-65319085-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319085
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319085
    reference: chr 5
allele count: 2
allele frequency: 1.649729444371123e-5
allele num: 121232
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.598-33A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.598-33A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.386A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.598-33A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.598-33A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.598-33A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.598-33A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.598-33A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.598-33A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.598-33A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.598-33A>C
  variant of: http://identifiers.org/hgnc/15842
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9158
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9501
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11231
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7421
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD

5-65319096-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319096
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319095
    reference: chr 5
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.598-18delC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.598-18delC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.598-18delC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.401delC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.598-18delC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.598-18delC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.598-18delC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.598-18delC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.598-18delC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.598-18delC
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.598-18delC
  variant of: http://identifiers.org/hgnc/15842
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11264
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4900
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: TC
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD

5-65319099-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319099
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319099
    reference: chr 5
allele count: 14
allele frequency: 1.153706694795135e-4
allele num: 121348
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.598-19C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.598-19C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.598-19C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.598-19C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.598-19C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.400C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.598-19C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.598-19C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.598-19C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.598-19C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.598-19C>T
  variant of: http://identifiers.org/hgnc/15842
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9510
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2501
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1422
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4884
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

5-65319100-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319100
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319100
    reference: chr 5
allele count: 2
allele frequency: 1.647907980818351e-5
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.598-18C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.598-18C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.598-18C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.598-18C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.598-18C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.598-18C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.401C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.598-18C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.598-18C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.598-18C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.598-18C>G
  variant of: http://identifiers.org/hgnc/15842
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5262
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6562
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD

5-65319107-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319107
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319107
    reference: chr 5
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.598-11A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.598-11A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.408A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.598-11A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.598-11A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.598-11A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.598-11A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.598-11A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.598-11A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.598-11A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.598-11A>T
  variant of: http://identifiers.org/hgnc/15842
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

5-65319114-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319114
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319114
    reference: chr 5
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.598-4A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.598-4A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.598-4A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.598-4A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.598-4A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.598-4A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.598-4A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.415A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.598-4A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.598-4A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.598-4A>G
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.598-4A>G
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

5-65319115-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319115
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319115
    reference: chr 5
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.598-3C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.598-3C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.598-3C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.598-3C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.598-3C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.598-3C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.598-3C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.598-3C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.598-3C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.598-3C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.416C>T
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7416
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.598-3C>T
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

5-65319144-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319144
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319144
    reference: chr 5
allele count: 4
allele frequency: 3.294784356363876e-5
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.624A>G
  hgvsp: ENST00000284037.5:c.624A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.624A>G
  hgvsp: ENST00000380935.1:c.624A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.624A>G
  hgvsp: ENST00000380936.1:c.624A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.624A>G
  hgvsp: ENST00000511297.1:c.624A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.624A>G
  hgvsp: ENST00000380938.2:c.624A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.624A>G
  hgvsp: ENST00000416865.2:c.624A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.445A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.624A>G
  hgvsp: ENST00000380943.2:c.624A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.624A>G
  hgvsp: ENST00000506030.1:c.624A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.624A>G
  hgvsp: ENST00000380939.2:c.624A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.624A>G
  hgvsp: ENST00000508515.1:c.624A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3343
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Gly208Gly
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

5-65319153-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319153
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319153
    reference: chr 5
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.633G>A
  hgvsp: ENST00000508515.1:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.633G>A
  hgvsp: ENST00000416865.2:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.633G>A
  hgvsp: ENST00000380936.1:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.633G>A
  hgvsp: ENST00000511297.1:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.633G>A
  hgvsp: ENST00000380935.1:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.633G>A
  hgvsp: ENST00000284037.5:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.633G>A
  hgvsp: ENST00000380938.2:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.633G>A
  hgvsp: ENST00000506030.1:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.633G>A
  hgvsp: ENST00000380943.2:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.454G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.633G>A
  hgvsp: ENST00000380939.2:c.633G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu211Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD

5-65319154-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319154
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319154
    reference: chr 5
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.634T>C
  hgvsp: ENSP00000370322.1:p.Phe212Leu
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.634T>C
  hgvsp: ENSP00000370325.2:p.Phe212Leu
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.455T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.634T>C
  hgvsp: ENSP00000284037.4:p.Phe212Leu
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.634T>C
  hgvsp: ENSP00000422015.1:p.Phe212Leu
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.634T>C
  hgvsp: ENSP00000426632.1:p.Phe212Leu
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.634T>C
  hgvsp: ENSP00000422766.1:p.Phe212Leu
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.634T>C
  hgvsp: ENSP00000370323.1:p.Phe212Leu
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.634T>C
  hgvsp: ENSP00000397833.2:p.Phe212Leu
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.634T>C
  hgvsp: ENSP00000370326.2:p.Phe212Leu
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.634T>C
  hgvsp: ENSP00000370330.2:p.Phe212Leu
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Phe212Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

5-65319154-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319154
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319154
    reference: chr 5
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.634T>G
  hgvsp: ENSP00000370326.2:p.Phe212Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.634T>G
  hgvsp: ENSP00000426632.1:p.Phe212Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.634T>G
  hgvsp: ENSP00000284037.4:p.Phe212Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.634T>G
  hgvsp: ENSP00000370325.2:p.Phe212Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.634T>G
  hgvsp: ENSP00000370330.2:p.Phe212Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.634T>G
  hgvsp: ENSP00000370322.1:p.Phe212Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.634T>G
  hgvsp: ENSP00000422015.1:p.Phe212Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.455T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.634T>G
  hgvsp: ENSP00000422766.1:p.Phe212Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.634T>G
  hgvsp: ENSP00000370323.1:p.Phe212Val
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.634T>G
  hgvsp: ENSP00000397833.2:p.Phe212Val
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3342
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2496
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7420
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11278
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9334
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe212Val
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

5-65319165-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319165
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319165
    reference: chr 5
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.645T>C
  hgvsp: ENST00000380938.2:c.645T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.645T>C
  hgvsp: ENST00000380943.2:c.645T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.645T>C
  hgvsp: ENST00000380935.1:c.645T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.645T>C
  hgvsp: ENST00000380939.2:c.645T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.645T>C
  hgvsp: ENST00000380936.1:c.645T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.645T>C
  hgvsp: ENST00000511297.1:c.645T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.645T>C
  hgvsp: ENST00000284037.5:c.645T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.645T>C
  hgvsp: ENST00000508515.1:c.645T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.466T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.645T>C
  hgvsp: ENST00000506030.1:c.645T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.645T>C
  hgvsp: ENST00000416865.2:c.645T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp215Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

5-65319169-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319169
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319169
    reference: chr 5
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.649A>G
  hgvsp: ENSP00000426632.1:p.Asn217Asp
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.649A>G
  hgvsp: ENSP00000422766.1:p.Asn217Asp
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.649A>G
  hgvsp: ENSP00000370330.2:p.Asn217Asp
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.649A>G
  hgvsp: ENSP00000370323.1:p.Asn217Asp
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.649A>G
  hgvsp: ENSP00000370326.2:p.Asn217Asp
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.649A>G
  hgvsp: ENSP00000284037.4:p.Asn217Asp
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.649A>G
  hgvsp: ENSP00000370322.1:p.Asn217Asp
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.649A>G
  hgvsp: ENSP00000422015.1:p.Asn217Asp
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.649A>G
  hgvsp: ENSP00000370325.2:p.Asn217Asp
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.470A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.649A>G
  hgvsp: ENSP00000397833.2:p.Asn217Asp
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn217Asp
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

5-65319171-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319171
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319171
    reference: chr 5
allele count: 1
allele frequency: 8.238046594391538e-6
allele num: 121388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.651T>C
  hgvsp: ENST00000380938.2:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.472T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.651T>C
  hgvsp: ENST00000506030.1:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.651T>C
  hgvsp: ENST00000380935.1:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.651T>C
  hgvsp: ENST00000508515.1:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.651T>C
  hgvsp: ENST00000380939.2:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.651T>C
  hgvsp: ENST00000380943.2:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.651T>C
  hgvsp: ENST00000380936.1:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.651T>C
  hgvsp: ENST00000284037.5:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.651T>C
  hgvsp: ENST00000511297.1:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.651T>C
  hgvsp: ENST00000416865.2:c.651T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4859
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11275
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2493
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn217Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

5-65319187-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319187
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319187
    reference: chr 5
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.667C>T
  hgvsp: ENSP00000370323.1:p.Pro223Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.667C>T
  hgvsp: ENSP00000370326.2:p.Pro223Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.488C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.667C>T
  hgvsp: ENSP00000397833.2:p.Pro223Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.667C>T
  hgvsp: ENSP00000422015.1:p.Pro223Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.667C>T
  hgvsp: ENSP00000284037.4:p.Pro223Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.667C>T
  hgvsp: ENSP00000370322.1:p.Pro223Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.667C>T
  hgvsp: ENSP00000426632.1:p.Pro223Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.667C>T
  hgvsp: ENSP00000370330.2:p.Pro223Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.667C>T
  hgvsp: ENSP00000422766.1:p.Pro223Ser
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.667C>T
  hgvsp: ENSP00000370325.2:p.Pro223Ser
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4831
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7422
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2493
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11276
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro223Ser
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD

5-65319201-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319201
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319201
    reference: chr 5
allele count: 2
allele frequency: 1.647907980818351e-5
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.672+9A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.672+9A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.672+9A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.672+9A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.672+9A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.672+9A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.672+9A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.493+9A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.672+9A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.672+9A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.672+9A>G
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5259
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum

5-65319210-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319210
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319210
    reference: chr 5
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.672+18T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.672+18T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.493+18T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.672+18T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.672+18T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.672+18T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.672+18T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.672+18T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.672+18T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.672+18T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.672+18T>G
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11273
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4740
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

5-65319221-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319221
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319221
    reference: chr 5
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.672+29A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.672+29A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.672+29A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.672+29A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.672+29A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.672+29A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.493+29A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.672+29A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.672+29A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.672+29A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.672+29A>G
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9483
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9208
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3341
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

5-65319225-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319225
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319225
    reference: chr 5
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.672+33A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.672+33A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.493+33A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.672+33A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.672+33A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.672+33A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.672+33A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.672+33A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.672+33A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.672+33A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.672+33A>G
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5254
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9066
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

5-65319231-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319231
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319231
    reference: chr 5
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.672+39G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.672+39G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.672+39G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.493+39G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.672+39G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.672+39G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.672+39G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.672+39G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.672+39G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.672+39G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.672+39G>A
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5250
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11053
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7407
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP

5-65319235-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319235
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319236
    reference: chr 5
allele count: 1
allele frequency: 8.25559316436886e-6
allele num: 121130
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.672+44dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.672+44dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.672+44dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.672+44dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.672+44dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.672+44dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.493+44dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.672+44dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.672+44dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.672+44dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.672+44dupT
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9416
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8257
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3869
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10737
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/5-65319238-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319238
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319238
    reference: chr 5
allele count: 1
allele frequency: 8.260503229856763e-6
allele num: 121058
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.672+46C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.672+46C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.672+46C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.672+46C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.672+46C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.672+46C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.672+46C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.493+46C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.672+46C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.672+46C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.672+46C>A
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3339
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5244
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2160
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 970
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4647
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3808
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

http://identifiers.org/exac.variant/5-65319244-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65319244
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65319244
    reference: chr 5
allele count: 2
allele frequency: 1.654861984510492e-5
allele num: 120856
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.672+52A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.493+52A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.672+52A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.672+52A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.672+52A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.672+52A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.672+52A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.672+52A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.672+52A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.672+52A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.672+52A>C
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9542
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5426
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8206
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5226
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3334
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9137
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 708
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1420
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1476
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

5-65320084-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65320084
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65320084
    reference: chr 5
allele count: 8
allele frequency: 7.454203238851307e-5
allele num: 107322
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.673-50C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.673-50C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.673-50C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.673-50C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.673-50C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.673-50C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.494-50C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.673-50C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.673-50C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.673-50C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.673-50C>T
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8694
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12155
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9764
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5537
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5215
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

5-65320093-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65320093
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65320093
    reference: chr 5
allele count: 19
allele frequency: 1.758380069224647e-4
allele num: 108054
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.673-41A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.673-41A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.673-41A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.673-41A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.673-41A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.673-41A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.673-41A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.494-41A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.673-41A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.673-41A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.673-41A>G
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13322
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8194
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17311
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4615
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5337
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5659
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1224
  bin: 8.25e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum

5-65320103-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65320103
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65320103
    reference: chr 5
allele count: 1
allele frequency: 9.152480322167307e-6
allele num: 109260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.673-31G>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.673-31G>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.673-31G>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.673-31G>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.673-31G>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.673-31G>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.673-31G>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.673-31G>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.494-31G>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.673-31G>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.673-31G>C
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1559
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5213
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/5-65320108-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65320108
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65320108
    reference: chr 5
allele count: 1
allele frequency: 9.044208089139715e-6
allele num: 110568
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.673-26A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.494-26A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.673-26A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.673-26A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.673-26A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.673-26A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.673-26A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.673-26A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.673-26A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.673-26A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.673-26A>C
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4733
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3943
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14970
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1907
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

5-65320117-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65320117
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65320117
    reference: chr 5
allele count: 1
allele frequency: 8.837982111924206e-6
allele num: 113148
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.673-17T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.673-17T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.673-17T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.494-17T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.673-17T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.673-17T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.673-17T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.673-17T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.673-17T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.673-17T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.673-17T>C
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

5-65320118-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65320118
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65320119
    reference: chr 5
allele count: 826
allele frequency: 7.282666196438018e-3
allele num: 113420
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.673-9dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.494-9dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.673-9dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.673-9dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.673-9dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.673-9dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.673-9dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.673-9dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.673-9dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.673-9dupT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.673-9dupT
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3438
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6210
  bin: 3.25e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.75e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 3.75e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 15655
  bin: 2.75e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 1.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 27178
  bin: 2.25e1
  variant carriers: 92
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 1729
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 3
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

5-65320118-C-CTT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65320118
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65320120
    reference: chr 5
allele count: 1
allele frequency: 8.816787162757892e-6
allele num: 113420
alternate allele: CTT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.673-10_673-9dupTT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.673-10_673-9dupTT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.673-10_673-9dupTT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.673-10_673-9dupTT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.494-10_494-9dupTT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.673-10_673-9dupTT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.673-10_673-9dupTT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.673-10_673-9dupTT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.673-10_673-9dupTT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.673-10_673-9dupTT
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.673-10_673-9dupTT
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6210
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1956
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP

5-65320129-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65320129
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65320129
    reference: chr 5
allele count: 4
allele frequency: 3.42448161909491e-5
allele num: 116806
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.673-5T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.673-5T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.673-5T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.673-5T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.494-5T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.673-5T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.673-5T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.673-5T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.673-5T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.673-5T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.673-5T>C
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29412
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1957
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.673-5T>C
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

5-65320131-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65320131
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65320131
    reference: chr 5
allele count: 3
allele frequency: 2.555627491736805e-5
allele num: 117388
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.673-3T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.673-3T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.494-3T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.673-3T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.673-3T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.673-3T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.673-3T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.673-3T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.673-3T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.673-3T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.673-3T>C
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29719
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.673-3T>C
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD

5-65320142-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65320142
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65320142
    reference: chr 5
allele count: 8
allele frequency: 6.711634618611363e-5
allele num: 119196
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.681T>C
  hgvsp: ENST00000380936.1:c.681T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.681T>C
  hgvsp: ENST00000284037.5:c.681T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000507128
  gene symbol: ERBB2IP
  hgvsc: ENST00000507128.1:n.502T>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.681T>C
  hgvsp: ENST00000506030.1:c.681T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.681T>C
  hgvsp: ENST00000511297.1:c.681T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.681T>C
  hgvsp: ENST00000380938.2:c.681T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.681T>C
  hgvsp: ENST00000380943.2:c.681T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.681T>C
  hgvsp: ENST00000380939.2:c.681T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.681T>C
  hgvsp: ENST00000508515.1:c.681T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.681T>C
  hgvsp: ENST00000380935.1:c.681T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.681T>C
  hgvsp: ENST00000416865.2:c.681T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30619
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly227Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

GenotypeQuality
all individuals: 3641
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4829
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1178
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4499
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3257
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1682
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5580
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12085
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1207
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.001201441730076e-4
allele num: 9988
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23794
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2110
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4114
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6786
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2134
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.27e-1

DP
type: SiteQuality
SIO_000300: 7.1269e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.83e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
type: SiteQuality
SIO_000300: 1.503e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.16e0

GenotypeQuality
all individuals: 238
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4499
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2720
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4829
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12085
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3257
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1207
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5580
bin: 1.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4114
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9988
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2134
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6786
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23794
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2110
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.16e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 7.1269e5

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

QD
type: SiteQuality
SIO_000300: 1.503e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.83e-2

GenotypeQuality
all individuals: 959
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3114
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4474
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11304
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8850
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5036
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1680
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5069
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8710
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 6.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6178
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1966
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21706
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3886
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1932
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 410
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.09194e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.64e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.323e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

GenotypeQuality
all individuals: 1265
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3116
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5005
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11360
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1681
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 727
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9049
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2714
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1970
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 21836
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6230
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3898
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1934
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

MQ
type: SiteQuality
SIO_000300: 4.196e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.68e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.916e0

QD
type: SiteQuality
SIO_000300: 1.357e1

DP
type: SiteQuality
SIO_000300: 7.09364e5

GenotypeQuality
all individuals: 411
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6279
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 425
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 9881
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2788
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9941
bin: 9.75e1
variant carriers: 85

GenotypeQuality
all individuals: 197
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3074
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3069
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1530
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 787
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4684
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1019
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2061
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1037
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 1.856665428889714e-4
allele num: 10772
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6308
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.313452617627568e-4
allele num: 15090
num of homozygotes: 0

East Asian
type: Population
allele count: 82
allele frequency: 1.045118531735916e-2
allele num: 7846
num of homozygotes: 3

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59280
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9378
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.347417840375587e-3
allele num: 852
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.38e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.22e0

FS
type: SiteQuality
SIO_000300: 2.024e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

QD
type: SiteQuality
SIO_000300: 1.591e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.38e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.63e-1

DP
type: SiteQuality
SIO_000300: 1.524037e6

GenotypeQuality
all individuals: 1053
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3050
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2717
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 790
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5981
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3547
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2929
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 396
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5876
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1544
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1035
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12575
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.689531661823343e-5
allele num: 59188
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10758
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15092
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6304
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.547770700636942e-4
allele num: 7850
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9374
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

QD
type: SiteQuality
SIO_000300: 3.34e0

MQRankSum
type: SiteQuality
SIO_000300: 1.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.804e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.539924e6

VQSLOD
type: SiteQuality
SIO_000300: -1.446e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.19e-1

GenotypeQuality
all individuals: 5626
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6043
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5361
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2613
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 292
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 813
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3141
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2946
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1120
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9877
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 564
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15140
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1087
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1614
bin: 7.75e1
variant carriers: 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
allele num: 9412
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10816
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6330
num of homozygotes: 0

South Asian
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allele count: 8
allele frequency: 5.288207297726071e-4
allele num: 15128
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.682595234890295e-5
allele num: 59432
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.68e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.55701e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.72e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.39e-1

QD
type: SiteQuality
SIO_000300: 1.218e1

VQSLOD
type: SiteQuality
SIO_000300: 4.72e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6346
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59924
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.582411795681937e-5
allele num: 15192
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10878
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

DP
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

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

MQRankSum
type: SiteQuality
SIO_000300: -1.16e-1

FS
type: SiteQuality
SIO_000300: 2.0771e1

VQSLOD
type: SiteQuality
SIO_000300: -3.21e0

BaseQRankSum
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SIO_000300: 2.24e0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15562
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.005763688760806e-5
allele num: 11104
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9772
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62516
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8358
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.4e0

FS
type: SiteQuality
SIO_000300: 1.205e0

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.46e-1

DP
type: SiteQuality
SIO_000300: 1.727137e6

ClippingRankSum
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SIO_000300: 1.48e0

ReadPosRankSum
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SIO_000300: 1.42e0

QD
type: SiteQuality
SIO_000300: 1.281e1

MQ
type: SiteQuality
SIO_000300: 5.912e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10114
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.239860227130913e-5
allele num: 16026
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.82e-1

QD
type: SiteQuality
SIO_000300: 1.259e1

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-1

FS
type: SiteQuality
SIO_000300: 3.32e0

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.792209e6

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 1131
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 72

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65038
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16062
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

African
type: Population
allele count: 71
allele frequency: 6.982690794649882e-3
allele num: 10168
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 3
allele frequency: 4.581551618814905e-4
allele num: 6548
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.507e1

MQ
type: SiteQuality
SIO_000300: 5.966e1

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

FS
type: SiteQuality
SIO_000300: 5.649999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.72e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.89e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.56e-1

DP
type: SiteQuality
SIO_000300: 1.80032e6

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.168497312456181e-4
allele num: 8558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65334
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11382
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16152
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.172e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-1

FS
type: SiteQuality
SIO_000300: 4.675e0

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.002e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.01e-1

DP
type: SiteQuality
SIO_000300: 1.809576e6

QD
type: SiteQuality
SIO_000300: 7.48e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1997
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.16370808678501e-5
allele num: 16224
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.5e-1

QD
type: SiteQuality
SIO_000300: 1.003e1

MQ
type: SiteQuality
SIO_000300: 5.956e1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -2.85e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.43e-1

DP
type: SiteQuality
SIO_000300: 1.822078e6

VQSLOD
type: SiteQuality
SIO_000300: 4.52e-1

GenotypeQuality
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variant carriers: 21

GenotypeQuality
all individuals: 54
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GenotypeQuality
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GenotypeQuality
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variant carriers: 469

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 264

GenotypeQuality
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GenotypeQuality
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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: 36

GenotypeQuality
all individuals: 1201
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variant carriers: 1060

GenotypeQuality
all individuals: 48549
bin: 9.75e1
variant carriers: 48178

East Asian
type: Population
allele count: 4450
allele frequency: 5.172013017201301e-1
allele num: 8604
num of homozygotes: 1141

Other
type: Population
allele count: 735
allele frequency: 8.112582781456954e-1
allele num: 906
num of homozygotes: 303

Latino
type: Population
allele count: 6079
allele frequency: 5.288846354619802e-1
allele num: 11494
num of homozygotes: 1689

European (Non-Finnish)
type: Population
allele count: 56758
allele frequency: 8.529906822963631e-1
allele num: 66540
num of homozygotes: 24226

African
type: Population
allele count: 5478
allele frequency: 5.283564814814815e-1
allele num: 10368
num of homozygotes: 1472

South Asian
type: Population
allele count: 14097
allele frequency: 8.5591985428051e-1
allele num: 16470
num of homozygotes: 6059

European (Finnish)
type: Population
allele count: 5652
allele frequency: 8.561042108451984e-1
allele num: 6602
num of homozygotes: 2423

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.732e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.255e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.19e-1

QD
type: SiteQuality
SIO_000300: 2.508e1

DP
type: SiteQuality
SIO_000300: 3.228923e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.49e-1

GenotypeQuality
all individuals: 254
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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
all individuals: 175
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.518326197200206e-5
allele num: 65862
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

South Asian
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allele frequency: 0.0e0
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ClippingRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
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DP
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SIO_000300: 1.856072e6

FS
type: SiteQuality
SIO_000300: 1.489e0

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 2.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.02e0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.517957436473481e-5
allele num: 65878
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
allele num: 10310
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South Asian
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VQSLOD
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DP
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FS
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11424
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.520958812435359e-5
allele num: 65748
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 888
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East Asian
type: Population
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allele frequency: 0.0e0
allele num: 8584
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African
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allele frequency: 0.0e0
allele num: 10308
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South Asian
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allele frequency: 1.844111138431276e-4
allele num: 16268
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European (Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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MQRankSum
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QD
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ClippingRankSum
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FS
type: SiteQuality
SIO_000300: 9.91e-1

ReadPosRankSum
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BaseQRankSum
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SIO_000300: -2.377e0

MQ
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SIO_000300: 6.0e1

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.518e-1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528210770829513e-5
allele num: 65436
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16206
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FS
type: SiteQuality
SIO_000300: 9.419999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.442e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.9e1

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.837583e6

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 4.45e-1

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

European (Finnish)
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allele count: 8
allele frequency: 1.218769043266301e-3
allele num: 6564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 65
allele frequency: 9.975445058317987e-4
allele num: 65160
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.194251734390486e-5
allele num: 16144
num of homozygotes: 0

Latino
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allele count: 5
allele frequency: 4.399859204505456e-4
allele num: 11364
num of homozygotes: 1

East Asian
type: Population
allele count: 1
allele frequency: 1.170411985018727e-4
allele num: 8544
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
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allele count: 2
allele frequency: 1.953506544246923e-4
allele num: 10238
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InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

ClippingRankSum
type: SiteQuality
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MQ
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BaseQRankSum
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VQSLOD
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QD
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 1.823939e6

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

Latino
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.07370750599373e-5
allele num: 65068
num of homozygotes: 0

African
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South Asian
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allele num: 16128
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Other
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allele count: 0
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allele num: 888
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6554
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DP
type: SiteQuality
SIO_000300: 1.819098e6

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

East Asian
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allele count: 1
allele frequency: 1.186239620403321e-4
allele num: 8430
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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DP
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FS
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ReadPosRankSum
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VQSLOD
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
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Other
type: Population
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Latino
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
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East Asian
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allele num: 8328
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European (Finnish)
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allele count: 0
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DP
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SIO_000300: 1.655765e6

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62626
num of homozygotes: 0

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

Latino
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allele frequency: 2.691548537591961e-4
allele num: 11146
num of homozygotes: 0

Other
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.524e0

BaseQRankSum
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ClippingRankSum
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SIO_000300: 1.8e-1

InbreedingCoeff
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QD
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MQ
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DP
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VQSLOD
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 61962
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East Asian
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allele frequency: 0.0e0
allele num: 8192
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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allele frequency: 1.025851456709069e-4
allele num: 9748
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 858
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European (Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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FS
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MQ
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MQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele num: 61704
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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ReadPosRankSum
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SIO_000300: -6.929999999999999e-1

FS
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VQSLOD
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QD
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InbreedingCoeff
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MQ
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MQRankSum
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BaseQRankSum
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

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

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

South Asian
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allele frequency: 6.483402489626556e-5
allele num: 15424
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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MQRankSum
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SIO_000300: -3.241e0

ReadPosRankSum
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FS
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VQSLOD
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InbreedingCoeff
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MQ
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ClippingRankSum
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QD
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BaseQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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South Asian
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allele num: 15402
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European (Finnish)
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ReadPosRankSum
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DP
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QD
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FS
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ClippingRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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VQSLOD
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 2.073398299813394e-4
allele num: 9646
num of homozygotes: 0

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

South Asian
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European (Finnish)
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African
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European (Non-Finnish)
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East Asian
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Other
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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QD
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MQ
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MQRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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Other
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FS
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QD
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MQRankSum
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ReadPosRankSum
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DP
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQ
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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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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
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allele frequency: 6.810133478616181e-5
allele num: 14684
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6252
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-1

BaseQRankSum
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SIO_000300: 1.01e-1

InbreedingCoeff
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SIO_000300: -3.4e-3

FS
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QD
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MQRankSum
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SIO_000300: -3.016e0

ReadPosRankSum
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MQ
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SIO_000300: 4.454e1

VQSLOD
type: SiteQuality
SIO_000300: -3.69e-1

DP
type: SiteQuality
SIO_000300: 1.359516e6

GenotypeQuality
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variant carriers: 0

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.162790697674419e-4
allele num: 8600
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Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66618
num of homozygotes: 0

ClippingRankSum
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SIO_000300: 1.14e0

DP
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VQSLOD
type: SiteQuality
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MQRankSum
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ReadPosRankSum
type: SiteQuality
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QD
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BaseQRankSum
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SIO_000300: 2.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
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SIO_000300: 0.0e0

MQ
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SIO_000300: 5.938e1

GenotypeQuality
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variant carriers: 1

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50159168718842e-5
allele num: 66596
num of homozygotes: 0

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

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

MQRankSum
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SIO_000300: 8.93e-1

InbreedingCoeff
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ClippingRankSum
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SIO_000300: 2.53e0

FS
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VQSLOD
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QD
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: -1.537e0

DP
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MQ
type: SiteQuality
SIO_000300: 5.909e1

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10360
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5008254539997e-5
allele num: 66630
num of homozygotes: 0

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

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

InbreedingCoeff
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SIO_000300: 1.0e-3

FS
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 4.6e-1

VQSLOD
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.937e1

DP
type: SiteQuality
SIO_000300: 2.621723e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.61e-1

QD
type: SiteQuality
SIO_000300: 9.57e0

GenotypeQuality
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variant carriers: 0

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

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

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

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

Latino
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
allele num: 6604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500645277469312e-5
allele num: 66638
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.625869e6

BaseQRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: 1.1e-3

ReadPosRankSum
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FS
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QD
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

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

Latino
type: Population
allele count: 0
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num of homozygotes: 0

African
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allele frequency: 1.927525057825752e-4
allele num: 10376
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
allele num: 16502
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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FS
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ReadPosRankSum
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BaseQRankSum
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MQ
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MQRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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South Asian
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Latino
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African
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European (Non-Finnish)
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European (Finnish)
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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FS
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MQRankSum
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InbreedingCoeff
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MQ
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
type: Population
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num of homozygotes: 0

African
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allele frequency: 4.808617041738796e-4
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East Asian
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allele frequency: 6.947660954145438e-4
allele num: 8636
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South Asian
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allele count: 0
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.497211728728189e-5
allele num: 66708
num of homozygotes: 0

Other
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European (Finnish)
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allele frequency: 0.0e0
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DP
type: SiteQuality
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QD
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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FS
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MQRankSum
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele frequency: 0.0e0
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Latino
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European (Non-Finnish)
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South Asian
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African
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European (Finnish)
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Other
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QD
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQ
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MQRankSum
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FS
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Other
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ClippingRankSum
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SIO_000300: 5.7e-2

FS
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VQSLOD
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ReadPosRankSum
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MQRankSum
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MQ
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SIO_000300: 5.962e1

InbreedingCoeff
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 2.67e0

DP
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SIO_000300: 2.632561e6

QD
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SIO_000300: 7.47e0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498531439189594e-5
allele num: 66732
num of homozygotes: 0

Other
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num of homozygotes: 0

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

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

ClippingRankSum
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SIO_000300: 6.879999999999999e-1

DP
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FS
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VQSLOD
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ReadPosRankSum
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MQRankSum
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QD
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BaseQRankSum
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MQ
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InbreedingCoeff
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SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Other
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num of homozygotes: 0

South Asian
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BaseQRankSum
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InbreedingCoeff
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QD
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VQSLOD
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DP
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FS
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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SIO_000300: 5.931e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele num: 66724
num of homozygotes: 0

Latino
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African
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South Asian
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FS
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ClippingRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Other
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num of homozygotes: 0

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

African
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66718
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499790029395885e-5
allele num: 66676
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.051e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 9.086e0

MQRankSum
type: SiteQuality
SIO_000300: 5.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.508e1

DP
type: SiteQuality
SIO_000300: 2.625249e6

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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bin: 7.75e1
variant carriers: 0

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

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

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

Latino
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allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

DP
type: SiteQuality
SIO_000300: 2.620876e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 5.13e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -5.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.74e-1

GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -4.893e0

QD
type: SiteQuality
SIO_000300: 1.606e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.374e0

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.948e1

MQRankSum
type: SiteQuality
SIO_000300: -2.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

DP
type: SiteQuality
SIO_000300: 2.612552e6

GenotypeQuality
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bin: 1.75e1
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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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: 2774
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.067224851352991e-5
allele num: 16482
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.602309e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.75e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.14e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.106e0

MQ
type: SiteQuality
SIO_000300: 6.03e1

QD
type: SiteQuality
SIO_000300: 1.41e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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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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bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.665571235260003e-5
allele num: 10346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66562
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.458e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.88e-1

FS
type: SiteQuality
SIO_000300: 1.674e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.595752e6

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10314
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.659508139937652e-5
allele num: 11548
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505298651252408e-5
allele num: 66432
num of homozygotes: 0

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

GenotypeQuality
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variant carriers: 0

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

African
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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: 11242
num of homozygotes: 0

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

East Asian
type: Population
allele count: 8
allele frequency: 1.003009027081244e-3
allele num: 7976
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59630
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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Other
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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DP
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FS
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MQ
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QD
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
type: Population
allele count: 0
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allele num: 8028
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 3.135779241141424e-4
allele num: 12756
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.857395925597875e-5
allele num: 11290
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 14
allele frequency: 2.334812047630166e-4
allele num: 59962
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8740
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
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QD
type: SiteQuality
SIO_000300: 1.73e1

DP
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
type: SiteQuality
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MQ
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FS
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3289
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11320
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8850
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8102
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.648261084555794e-5
allele num: 60670
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13014
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.92e-1

DP
type: SiteQuality
SIO_000300: 1.453638e6

QD
type: SiteQuality
SIO_000300: 6.74e0

FS
type: SiteQuality
SIO_000300: 7.975e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.335e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.174e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.92e-1

GenotypeQuality
all individuals: 99
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1715
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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
all individuals: 3291
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5900
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.479431563201197e-5
allele num: 13370
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8966
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6478
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8176
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61368
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 7.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.73e-1

DP
type: SiteQuality
SIO_000300: 1.485437e6

MQRankSum
type: SiteQuality
SIO_000300: -5.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.04e-1

QD
type: SiteQuality
SIO_000300: 1.218e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.41e0

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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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
all individuals: 3290
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 700
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GenotypeQuality
all individuals: 6132
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14172
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.594642002870356e-5
allele num: 62710
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9150
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8316
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.668e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.679999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.529714e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.149999999999999e-1

QD
type: SiteQuality
SIO_000300: 2.015e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.78e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

GenotypeQuality
all individuals: 352
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 453
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variant carriers: 1

GenotypeQuality
all individuals: 37155
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4035
bin: 9.75e1
variant carriers: 813

GenotypeQuality
all individuals: 196
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 65
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 683
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variant carriers: 0

GenotypeQuality
all individuals: 3564
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 339
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1251
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 6048
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 203
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2048
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 359
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 22
allele frequency: 3.370098039215686e-3
allele num: 6528
num of homozygotes: 0

African
type: Population
allele count: 12
allele frequency: 1.30890052356021e-3
allele num: 9168
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.201345506967804e-4
allele num: 8324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 650
allele frequency: 1.033452047824981e-2
allele num: 62896
num of homozygotes: 3

Latino
type: Population
allele count: 42
allele frequency: 3.674540682414698e-3
allele num: 11430
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 4.705882352941176e-3
allele num: 850
num of homozygotes: 0

South Asian
type: Population
allele count: 95
allele frequency: 6.678852643419573e-3
allele num: 14224
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

FS
type: SiteQuality
SIO_000300: 7.05e-1

MQ
type: SiteQuality
SIO_000300: 6.035e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.117e1

DP
type: SiteQuality
SIO_000300: 1.545847e6

VQSLOD
type: SiteQuality
SIO_000300: 4.63e0

GenotypeQuality
all individuals: 87
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 359
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variant carriers: 0

GenotypeQuality
all individuals: 65
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GenotypeQuality
all individuals: 489
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variant carriers: 0

GenotypeQuality
all individuals: 352
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GenotypeQuality
all individuals: 37155
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variant carriers: 0

GenotypeQuality
all individuals: 687
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 683
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variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1729
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2048
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3564
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1251
bin: 8.25e1
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GenotypeQuality
all individuals: 4035
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 339
bin: 5.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14224
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9168
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.589926227423048e-5
allele num: 62896
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.63e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.56e-1

FS
type: SiteQuality
SIO_000300: 7.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.399999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

MQ
type: SiteQuality
SIO_000300: 6.035e1

QD
type: SiteQuality
SIO_000300: 1.117e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.545847e6

GenotypeDepth
all individuals: 43
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variant carriers: 0

GenotypeQuality
all individuals: 1829
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variant carriers: 0

GenotypeQuality
all individuals: 88
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 722
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GenotypeQuality
all individuals: 93
bin: 5.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.594706798131811e-4
allele num: 15416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64570
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.576224e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.11e0

FS
type: SiteQuality
SIO_000300: 2.391e0

QD
type: SiteQuality
SIO_000300: 1.202e1

MQRankSum
type: SiteQuality
SIO_000300: -1.81e-1

InbreedingCoeff
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SIO_000300: 1.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.27e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

VQSLOD
type: SiteQuality
SIO_000300: 7.85e-1

GenotypeDepth
all individuals: 378
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 138
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 79
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1337
bin: 8.25e1
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GenotypeQuality
all individuals: 725
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.08461087633795e-5
allele num: 64838
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.056189269117026e-4
allele num: 9468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15612
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.209e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

DP
type: SiteQuality
SIO_000300: 1.582818e6

MQRankSum
type: SiteQuality
SIO_000300: 4.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.931e1

VQSLOD
type: SiteQuality
SIO_000300: 2.91e-1

QD
type: SiteQuality
SIO_000300: 1.657e1

GenotypeDepth
all individuals: 188
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 929
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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GenotypeQuality
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GenotypeQuality
all individuals: 108
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 11
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GenotypeQuality
all individuals: 6706
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GenotypeQuality
all individuals: 59
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GenotypeQuality
all individuals: 46
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GenotypeQuality
all individuals: 42372
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GenotypeQuality
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GenotypeQuality
all individuals: 50
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GenotypeQuality
all individuals: 1367
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GenotypeQuality
all individuals: 732
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GenotypeQuality
all individuals: 1880
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GenotypeQuality
all individuals: 36
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GenotypeQuality
all individuals: 3289
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 521
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variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2249
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65714
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9702
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16200
num of homozygotes: 0

East Asian
type: Population
allele count: 8
allele frequency: 9.321836401771149e-4
allele num: 8582
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -7.64e-1

DP
type: SiteQuality
SIO_000300: 1.604535e6

QD
type: SiteQuality
SIO_000300: 1.123e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e-1

FS
type: SiteQuality
SIO_000300: 2.664e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.24e0

VQSLOD
type: SiteQuality
SIO_000300: 7.41e-1