5-65374261-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374261
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374261
    reference: chr 5
allele count: 15
allele frequency: 1.248772040826521e-4
allele num: 120118
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.385A>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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.552A>G
  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.3926A>G
  hgvsp: ENSP00000370323.1:p.Tyr1309Cys
  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.4019A>G
  hgvsp: ENSP00000370330.2:p.Tyr1340Cys
  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.4163A>G
  hgvsp: ENSP00000426632.1:p.Tyr1388Cys
  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.3986A>G
  hgvsp: ENSP00000370326.2:p.Tyr1329Cys
  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.4142A>G
  hgvsp: ENSP00000284037.4:p.Tyr1381Cys
  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.3812A>G
  hgvsp: ENSP00000370322.1:p.Tyr1271Cys
  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.1736A>G
  hgvsp: ENSP00000397833.2:p.Tyr579Cys
  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.4007A>G
  hgvsp: ENSP00000422766.1:p.Tyr1336Cys
  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.3944A>G
  hgvsp: ENSP00000370325.2:p.Tyr1315Cys
  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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.244A>G
  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.3812A>G
  hgvsp: ENSP00000422015.1:p.Tyr1271Cys
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8847
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Tyr1388Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/5-65374262-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374262
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374262
    reference: chr 5
allele count: 1639
allele frequency: 1.393115172120697e-2
allele num: 117650
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.1737C>A
  hgvsp: ENSP00000397833.2:p.Tyr579Ter
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.4143C>A
  hgvsp: ENSP00000284037.4:p.Tyr1381Ter
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.3927C>A
  hgvsp: ENSP00000370323.1:p.Tyr1309Ter
  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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.386C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.3987C>A
  hgvsp: ENSP00000370326.2:p.Tyr1329Ter
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.3945C>A
  hgvsp: ENSP00000370325.2:p.Tyr1315Ter
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.4008C>A
  hgvsp: ENSP00000422766.1:p.Tyr1336Ter
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.3813C>A
  hgvsp: ENSP00000370322.1:p.Tyr1271Ter
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.4164C>A
  hgvsp: ENSP00000426632.1:p.Tyr1388Ter
  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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.553C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.3813C>A
  hgvsp: ENSP00000422015.1:p.Tyr1271Ter
  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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.245C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.4020C>A
  hgvsp: ENSP00000370330.2:p.Tyr1340Ter
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 5.25e1
  variant carriers: 118
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 6.25e1
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 5.75e1
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1165
  bin: 9.75e1
  variant carriers: 356
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 1.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3011
  bin: 3.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 4.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 3.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 8288
  bin: 2.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 8.25e1
  variant carriers: 114
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 4.75e1
  variant carriers: 96
genotype quality: GenotypeQuality
hgvs: p.Tyr1388Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

5-65374269-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374269
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374269
    reference: chr 5
allele count: 2
allele frequency: 1.660191918185742e-5
allele num: 120468
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.3820A>T
  hgvsp: ENSP00000422015.1:p.Ile1274Leu
  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.3820A>T
  hgvsp: ENSP00000370322.1:p.Ile1274Leu
  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.4150A>T
  hgvsp: ENSP00000284037.4:p.Ile1384Leu
  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.1744A>T
  hgvsp: ENSP00000397833.2:p.Ile582Leu
  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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.393A>T
  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.3934A>T
  hgvsp: ENSP00000370323.1:p.Ile1312Leu
  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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.252A>T
  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.4027A>T
  hgvsp: ENSP00000370330.2:p.Ile1343Leu
  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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.560A>T
  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.4015A>T
  hgvsp: ENSP00000422766.1:p.Ile1339Leu
  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.3994A>T
  hgvsp: ENSP00000370326.2:p.Ile1332Leu
  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.3952A>T
  hgvsp: ENSP00000370325.2:p.Ile1318Leu
  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.4171A>T
  hgvsp: ENSP00000426632.1:p.Ile1391Leu
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8759
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ile1391Leu
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

5-65374283-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374283
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374283
    reference: chr 5
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.3834T>C
  hgvsp: ENST00000380935.1:c.3834T>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.4041T>C
  hgvsp: ENST00000380943.2:c.4041T>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.4008T>C
  hgvsp: ENST00000380939.2:c.4008T>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.1758T>C
  hgvsp: ENST00000416865.2:c.1758T>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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.574T>C
  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.3966T>C
  hgvsp: ENST00000380938.2:c.3966T>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.3834T>C
  hgvsp: ENST00000508515.1:c.3834T>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.4164T>C
  hgvsp: ENST00000284037.5:c.4164T>C(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.4185T>C
  hgvsp: ENST00000506030.1:c.4185T>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.4029T>C
  hgvsp: ENST00000511297.1:c.4029T>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.3948T>C
  hgvsp: ENST00000380936.1:c.3948T>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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.407T>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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.266T>C
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His1395His
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

5-65374285-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374285
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374285
    reference: chr 5
allele count: 1
allele frequency: 8.279516476237788e-6
allele num: 120780
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.4031G>T
  hgvsp: ENSP00000422766.1:p.Gly1344Val
  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.3836G>T
  hgvsp: ENSP00000370322.1:p.Gly1279Val
  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.4187G>T
  hgvsp: ENSP00000426632.1:p.Gly1396Val
  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.3836G>T
  hgvsp: ENSP00000422015.1:p.Gly1279Val
  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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.409G>T
  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.4043G>T
  hgvsp: ENSP00000370330.2:p.Gly1348Val
  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.1760G>T
  hgvsp: ENSP00000397833.2:p.Gly587Val
  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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.576G>T
  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.4166G>T
  hgvsp: ENSP00000284037.4:p.Gly1389Val
  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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.268G>T
  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.3950G>T
  hgvsp: ENSP00000370323.1:p.Gly1317Val
  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.4010G>T
  hgvsp: ENSP00000370326.2:p.Gly1337Val
  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.3968G>T
  hgvsp: ENSP00000370325.2:p.Gly1323Val
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39502
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3422
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly1396Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

5-65374286-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374286
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374286
    reference: chr 5
allele count: 1
allele frequency: 8.279242283746192e-6
allele num: 120784
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.4011A>G
  hgvsp: ENST00000380939.2:c.4011A>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.4032A>G
  hgvsp: ENST00000511297.1:c.4032A>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.3837A>G
  hgvsp: ENST00000380935.1:c.3837A>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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.410A>G
  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.4188A>G
  hgvsp: ENST00000506030.1:c.4188A>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.3951A>G
  hgvsp: ENST00000380936.1:c.3951A>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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.577A>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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.269A>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.4044A>G
  hgvsp: ENST00000380943.2:c.4044A>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.3969A>G
  hgvsp: ENST00000380938.2:c.3969A>G(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.4167A>G
  hgvsp: ENST00000284037.5:c.4167A>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.3837A>G
  hgvsp: ENST00000508515.1:c.3837A>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.1761A>G
  hgvsp: ENST00000416865.2:c.1761A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39509
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly1396Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ

http://identifiers.org/exac.variant/5-65374306-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374306
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374306
    reference: chr 5
allele count: 1
allele frequency: 8.270204108637402e-6
allele num: 120916
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.3971A>C
  hgvsp: ENSP00000370323.1:p.Lys1324Thr
  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.3857A>C
  hgvsp: ENSP00000422015.1:p.Lys1286Thr
  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.4187A>C
  hgvsp: ENSP00000284037.4:p.Lys1396Thr
  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.4052A>C
  hgvsp: ENSP00000422766.1:p.Lys1351Thr
  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.3857A>C
  hgvsp: ENSP00000370322.1:p.Lys1286Thr
  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.1781A>C
  hgvsp: ENSP00000397833.2:p.Lys594Thr
  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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.430A>C
  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.4031A>C
  hgvsp: ENSP00000370326.2:p.Lys1344Thr
  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.4064A>C
  hgvsp: ENSP00000370330.2:p.Lys1355Thr
  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.3989A>C
  hgvsp: ENSP00000370325.2:p.Lys1330Thr
  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.4208A>C
  hgvsp: ENSP00000426632.1:p.Lys1403Thr
  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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.597A>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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.289A>C
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3408
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys1403Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

5-65374312-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374312
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374312
    reference: chr 5
allele count: 1
allele frequency: 8.270067318347971e-6
allele num: 120918
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.3977T>C
  hgvsp: ENSP00000370323.1:p.Phe1326Ser
  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.3863T>C
  hgvsp: ENSP00000422015.1:p.Phe1288Ser
  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.4058T>C
  hgvsp: ENSP00000422766.1:p.Phe1353Ser
  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.1787T>C
  hgvsp: ENSP00000397833.2:p.Phe596Ser
  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.4214T>C
  hgvsp: ENSP00000426632.1:p.Phe1405Ser
  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.4193T>C
  hgvsp: ENSP00000284037.4:p.Phe1398Ser
  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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.436T>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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.295T>C
  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.3863T>C
  hgvsp: ENSP00000370322.1:p.Phe1288Ser
  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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.603T>C
  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.4037T>C
  hgvsp: ENSP00000370326.2:p.Phe1346Ser
  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.3995T>C
  hgvsp: ENSP00000370325.2:p.Phe1332Ser
  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.4070T>C
  hgvsp: ENSP00000370330.2:p.Phe1357Ser
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe1405Ser
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

5-65374313-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374313
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374313
    reference: chr 5
allele count: 1
allele frequency: 8.270888127967181e-6
allele num: 120906
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.4059C>G
  hgvsp: ENSP00000422766.1:p.Phe1353Leu
  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.3864C>G
  hgvsp: ENSP00000422015.1:p.Phe1288Leu
  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.4215C>G
  hgvsp: ENSP00000426632.1:p.Phe1405Leu
  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.3996C>G
  hgvsp: ENSP00000370325.2:p.Phe1332Leu
  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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.604C>G
  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.3864C>G
  hgvsp: ENSP00000370322.1:p.Phe1288Leu
  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.4194C>G
  hgvsp: ENSP00000284037.4:p.Phe1398Leu
  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.1788C>G
  hgvsp: ENSP00000397833.2:p.Phe596Leu
  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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.296C>G
  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.4038C>G
  hgvsp: ENSP00000370326.2:p.Phe1346Leu
  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.3978C>G
  hgvsp: ENSP00000370323.1:p.Phe1326Leu
  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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.437C>G
  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.4071C>G
  hgvsp: ENSP00000370330.2:p.Phe1357Leu
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39395
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe1405Leu
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

5-65374320-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374320
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374320
    reference: chr 5
allele count: 1
allele frequency: 8.272667107875579e-6
allele num: 120880
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.3871A>G
  hgvsp: ENSP00000370322.1:p.Thr1291Ala
  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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.303A>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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.444A>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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.611A>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.4066A>G
  hgvsp: ENSP00000422766.1:p.Thr1356Ala
  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.3985A>G
  hgvsp: ENSP00000370323.1:p.Thr1329Ala
  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.1795A>G
  hgvsp: ENSP00000397833.2:p.Thr599Ala
  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.4078A>G
  hgvsp: ENSP00000370330.2:p.Thr1360Ala
  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.4045A>G
  hgvsp: ENSP00000370326.2:p.Thr1349Ala
  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.4222A>G
  hgvsp: ENSP00000426632.1:p.Thr1408Ala
  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.4003A>G
  hgvsp: ENSP00000370325.2:p.Thr1335Ala
  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.3871A>G
  hgvsp: ENSP00000422015.1:p.Thr1291Ala
  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.4201A>G
  hgvsp: ENSP00000284037.4:p.Thr1401Ala
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9086
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr1408Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum

5-65374321-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374321
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374321
    reference: chr 5
allele count: 1
allele frequency: 8.274720728175424e-6
allele num: 120850
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.612C>T
  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.3872C>T
  hgvsp: ENSP00000370322.1:p.Thr1291Ile
  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.4067C>T
  hgvsp: ENSP00000422766.1:p.Thr1356Ile
  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.4202C>T
  hgvsp: ENSP00000284037.4:p.Thr1401Ile
  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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.304C>T
  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.4004C>T
  hgvsp: ENSP00000370325.2:p.Thr1335Ile
  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.3986C>T
  hgvsp: ENSP00000370323.1:p.Thr1329Ile
  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.4046C>T
  hgvsp: ENSP00000370326.2:p.Thr1349Ile
  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.3872C>T
  hgvsp: ENSP00000422015.1:p.Thr1291Ile
  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.4223C>T
  hgvsp: ENSP00000426632.1:p.Thr1408Ile
  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.4079C>T
  hgvsp: ENSP00000370330.2:p.Thr1360Ile
  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.1796C>T
  hgvsp: ENSP00000397833.2:p.Thr599Ile
  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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.445C>T
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39257
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr1408Ile
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

5-65374338-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374338
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374338
    reference: chr 5
allele count: 1
allele frequency: 8.285416010737898e-6
allele num: 120694
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.629G>A
  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.1813G>A
  hgvsp: ENSP00000397833.2:p.Val605Ile
  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.4003G>A
  hgvsp: ENSP00000370323.1:p.Val1335Ile
  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.4021G>A
  hgvsp: ENSP00000370325.2:p.Val1341Ile
  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.3889G>A
  hgvsp: ENSP00000422015.1:p.Val1297Ile
  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.4063G>A
  hgvsp: ENSP00000370326.2:p.Val1355Ile
  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.3889G>A
  hgvsp: ENSP00000370322.1:p.Val1297Ile
  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.4240G>A
  hgvsp: ENSP00000426632.1:p.Val1414Ile
  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.4084G>A
  hgvsp: ENSP00000422766.1:p.Val1362Ile
  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.4219G>A
  hgvsp: ENSP00000284037.4:p.Val1407Ile
  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.4096G>A
  hgvsp: ENSP00000370330.2:p.Val1366Ile
  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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.321G>A
  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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.462G>A
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9158
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val1414Ile
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

5-65374341-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374341
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374341
    reference: chr 5
allele count: 1
allele frequency: 8.287613333112331e-6
allele num: 120662
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.3892C>T
  hgvsp: ENSP00000370322.1:p.Arg1298Ter
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.4243C>T
  hgvsp: ENSP00000426632.1:p.Arg1415Ter
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.4099C>T
  hgvsp: ENSP00000370330.2:p.Arg1367Ter
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.3892C>T
  hgvsp: ENSP00000422015.1:p.Arg1298Ter
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.4222C>T
  hgvsp: ENSP00000284037.4:p.Arg1408Ter
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.4024C>T
  hgvsp: ENSP00000370325.2:p.Arg1342Ter
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.1816C>T
  hgvsp: ENSP00000397833.2:p.Arg606Ter
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.4087C>T
  hgvsp: ENSP00000422766.1:p.Arg1363Ter
  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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.465C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.4066C>T
  hgvsp: ENSP00000370326.2:p.Arg1356Ter
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.4006C>T
  hgvsp: ENSP00000370323.1:p.Arg1336Ter
  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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.632C>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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.324C>T
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9190
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38834
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg1415Ter
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

5-65374356-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374356
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374357
    reference: chr 5
allele count: 1
allele frequency: 8.321821480285606e-6
allele num: 120166
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.341dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: frameshift_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.4041dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: stop_retained_variant
  consequence: frameshift_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.4260dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: frameshift_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.4239dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: frameshift_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.4104dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: frameshift_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.4116dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: frameshift_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.4083dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: frameshift_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.3909dupA
  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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.649dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: frameshift_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.3909dupA
  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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.482dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: frameshift_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.1833dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: frameshift_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.4023dupA
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9272
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2092
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37941
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/5-65374369-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374369
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374370
    reference: chr 5
allele count: 21
allele frequency: 1.76702231496752e-4
allele num: 118844
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.*18dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.*18dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.*18dupA
  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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.667dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.*18dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.*18dupA
  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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.500dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.*18dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.*18dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_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: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.*18dupA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.*18dupA
  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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.359dupA
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3865
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9295
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 34808
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 1
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/5-65374369-CA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374369
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374368
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 118844
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.359delA
  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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.667delA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.*18delA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.*18delA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.*18delA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.*18delA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.*18delA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.*18delA
  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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.500delA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.*18delA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_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: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.*18delA
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.*18delA
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: 3' UTR
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3865
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34808
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: CA
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/5-65374372-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374372
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374372
    reference: chr 5
allele count: 1
allele frequency: 8.408166010829718e-6
allele num: 118932
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.*14A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.*14A>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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.663A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.*14A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.*14A>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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.355A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.*14A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.*14A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.*14A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.*14A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.*14A>C
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422766
  ensembl transcript: ENST00000511297
  gene symbol: ERBB2IP
  hgvsc: ENST00000511297.1:c.*14A>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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.496A>C
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2088
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ

5-65374376-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374376
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374376
    reference: chr 5
allele count: 6
allele frequency: 5.063974882684582e-5
allele num: 118484
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.*18A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.*18A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.*18A>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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.667A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.*18A>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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.500A>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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.359A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.*18A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.*18A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.*18A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.*18A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.*18A>G
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3452
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4629
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP

5-65374377-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374377
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374377
    reference: chr 5
allele count: 13
allele frequency: 1.097787535889208e-4
allele num: 118420
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.*19G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.*19G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.*19G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.*19G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.*19G>A
  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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.501G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.*19G>A
  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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.668G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.*19G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.*19G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.*19G>A
  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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.360G>A
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32456
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9147
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1662
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3485
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2096
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

5-65374378-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374378
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374378
    reference: chr 5
allele count: 3
allele frequency: 2.536740457627979e-5
allele num: 118262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.502C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.*20C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.*20C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.*20C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.*20C>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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.669C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.*20C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.*20C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.*20C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.*20C>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.*20C>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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.361C>T
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9113
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31863
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

5-65374379-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374379
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374379
    reference: chr 5
allele count: 7
allele frequency: 5.930293634253376e-5
allele num: 118038
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.*21G>A
  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: ENST00000506744
  gene symbol: ERBB2IP
  hgvsc: ENST00000506744.1:n.670G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.*21G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.*21G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.*21G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.*21G>A
  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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.503G>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.*21G>A
  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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.362G>A
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1794
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8965
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6018
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

10-135193548-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135193548
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135193548
    reference: chr 10
allele count: 1
allele frequency: 9.336719450253958e-6
allele num: 107104
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.181+547G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.181+547G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.227G>T
  hgvsp: ENSP00000435514.1:p.Arg76Leu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.227G>T
  hgvsp: ENSP00000349847.3:p.Arg76Leu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.181+547G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.189G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.227G>T
  hgvsp: ENSP00000278060.5:p.Arg76Leu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.181+547G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.227G>T
  hgvsp: ENSP00000348654.5:p.Arg76Leu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000528127
  gene symbol: PAOX
  hgvsc: ENST00000528127.1:n.269G>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12562
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26476
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg76Leu
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

http://identifiers.org/exac.variant/5-65374387-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374387
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374387
    reference: chr 5
allele count: 9
allele frequency: 7.673550125334652e-5
allele num: 117286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.511C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.*29C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.*29C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.*29C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.*29C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.*29C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.*29C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.*29C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.*29C>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.*29C>A
  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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.370C>A
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26356
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3973
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8798
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8217
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3325
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5001
  bin: 9.75e1
  variant carriers: 9
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD

5-65374388-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374388
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374388
    reference: chr 5
allele count: 1
allele frequency: 8.527766407422568e-6
allele num: 117264
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112851
  ensembl transcript: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.371A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.*30A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.*30A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.*30A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000426632
  ensembl transcript: ENST00000506030
  gene symbol: ERBB2IP
  hgvsc: ENST00000506030.1:c.*30A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.*30A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.*30A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.*30A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.*30A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.*30A>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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.512A>G
  variant of: http://identifiers.org/hgnc/15842
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7918
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4997
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9398
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3256
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

5-65374394-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374394
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374394
    reference: chr 5
allele count: 11
allele frequency: 9.432344366317956e-5
allele num: 116620
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.*36A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.*36A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.*36A>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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.518A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.*36A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.*36A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.*36A>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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.377A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.*36A>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.*36A>G
  variant of: http://identifiers.org/hgnc/15842
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7145
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9691
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19934
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2967
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24118
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 1
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum

5-65374396-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374396
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374396
    reference: chr 5
allele count: 41
allele frequency: 3.523850451224753e-4
allele num: 116350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.*38T>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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.379T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.*38T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.*38T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.*38T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.*38T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.*38T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.*38T>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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.520T>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.*38T>G
  variant of: http://identifiers.org/hgnc/15842
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10477
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10828
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18922
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6956
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS

5-65374399-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374399
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374399
    reference: chr 5
allele count: 3
allele frequency: 2.583489777992112e-5
allele num: 116122
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.*41T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.*41T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.*41T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.*41T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.*41T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.*41T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.*41T>A
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.*41T>A
  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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.523T>A
  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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.382T>A
  variant of: http://identifiers.org/hgnc/15842
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16705
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13699
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1641
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19671
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1428
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 908
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

5-65374406-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374406
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374406
    reference: chr 5
allele count: 2
allele frequency: 1.769942830846564e-5
allele num: 112998
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.*48A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.*48A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.*48A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.*48A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.*48A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.*48A>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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.389A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.*48A>T
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.*48A>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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.530A>T
  variant of: http://identifiers.org/hgnc/15842
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14009
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9928
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16870
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7877
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1093
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4540
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1056
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

5-65374409-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65374409
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65374409
    reference: chr 5
allele count: 1
allele frequency: 9.070294784580499e-6
allele num: 110250
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000422015
  ensembl transcript: ENST00000508515
  gene symbol: ERBB2IP
  hgvsc: ENST00000508515.1:c.*51C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370322
  ensembl transcript: ENST00000380935
  gene symbol: ERBB2IP
  hgvsc: ENST00000380935.1:c.*51C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370330
  ensembl transcript: ENST00000380943
  gene symbol: ERBB2IP
  hgvsc: ENST00000380943.2:c.*51C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370326
  ensembl transcript: ENST00000380939
  gene symbol: ERBB2IP
  hgvsc: ENST00000380939.2:c.*51C>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: ENST00000509946
  gene symbol: ERBB2IP
  hgvsc: ENST00000509946.1:n.533C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000284037
  ensembl transcript: ENST00000284037
  gene symbol: ERBB2IP
  hgvsc: ENST00000284037.5:c.*51C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370323
  ensembl transcript: ENST00000380936
  gene symbol: ERBB2IP
  hgvsc: ENST00000380936.1:c.*51C>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: ENST00000503913
  gene symbol: ERBB2IP
  hgvsc: ENST00000503913.1:n.392C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000397833
  ensembl transcript: ENST00000416865
  gene symbol: ERBB2IP
  hgvsc: ENST00000416865.2:c.*51C>G
  variant of: http://identifiers.org/hgnc/15842
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112851
  ensembl protein: ENSP00000370325
  ensembl transcript: ENST00000380938
  gene symbol: ERBB2IP
  hgvsc: ENST00000380938.2:c.*51C>G
  variant of: http://identifiers.org/hgnc/15842
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13893
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9888
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1241
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6474
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3822
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

5-65440168-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65440168
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65440168
    reference: chr 5
allele count: 1
allele frequency: 5.833625014584062e-5
allele num: 17142
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153914
  ensembl protein: ENSP00000428272
  ensembl transcript: ENST00000521691
  gene symbol: SREK1
  hgvsc: ENST00000521691.1:c.-312+4329C>T
  variant of: http://identifiers.org/hgnc/17882
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153914
  ensembl transcript: ENST00000524111
  gene symbol: SREK1
  hgvsc: ENST00000524111.1:n.5C>T
  variant of: http://identifiers.org/hgnc/17882
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153914
  ensembl transcript: ENST00000520058
  gene symbol: SREK1
  hgvsc: ENST00000520058.1:n.34C>T
  variant of: http://identifiers.org/hgnc/17882
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000153914
  ensembl protein: ENSP00000334538
  ensembl transcript: ENST00000334121
  gene symbol: SREK1
  hgvsc: ENST00000334121.6:c.-37C>T
  variant of: http://identifiers.org/hgnc/17882
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000153914
  ensembl protein: ENSP00000428970
  ensembl transcript: ENST00000520953
  gene symbol: SREK1
  hgvsc: ENST00000520953.1:c.-37C>T
  variant of: http://identifiers.org/hgnc/17882
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153914
  ensembl transcript: ENST00000523851
  gene symbol: SREK1
  hgvsc: ENST00000523851.1:n.77C>T
  variant of: http://identifiers.org/hgnc/17882
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000153914
  ensembl protein: ENSP00000427935
  ensembl transcript: ENST00000522912
  gene symbol: SREK1
  hgvsc: ENST00000522912.1:c.-37C>T
  variant of: http://identifiers.org/hgnc/17882
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000253744
  ensembl transcript: ENST00000521596
  gene symbol: AC025442.3
  hgvsc: ENST00000521596.1:n.297G>A
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 970
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6186
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3380
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP

5-65440169-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 65440169
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 65440169
    reference: chr 5
allele count: 0
allele frequency: 0.0e0
allele num: 17328
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000153914
  ensembl protein: ENSP00000334538
  ensembl transcript: ENST00000334121
  gene symbol: SREK1
  hgvsc: ENST00000334121.6:c.-36G>A
  variant of: http://identifiers.org/hgnc/17882
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153914
  ensembl transcript: ENST00000523851
  gene symbol: SREK1
  hgvsc: ENST00000523851.1:n.78G>A
  variant of: http://identifiers.org/hgnc/17882
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000253744
  ensembl transcript: ENST00000521596
  gene symbol: AC025442.3
  hgvsc: ENST00000521596.1:n.296C>T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000153914
  ensembl protein: ENSP00000427935
  ensembl transcript: ENST00000522912
  gene symbol: SREK1
  hgvsc: ENST00000522912.1:c.-36G>A
  variant of: http://identifiers.org/hgnc/17882
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153914
  ensembl protein: ENSP00000428272
  ensembl transcript: ENST00000521691
  gene symbol: SREK1
  hgvsc: ENST00000521691.1:c.-312+4330G>A
  variant of: http://identifiers.org/hgnc/17882
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153914
  ensembl transcript: ENST00000520058
  gene symbol: SREK1
  hgvsc: ENST00000520058.1:n.35G>A
  variant of: http://identifiers.org/hgnc/17882
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000153914
  ensembl transcript: ENST00000524111
  gene symbol: SREK1
  hgvsc: ENST00000524111.1:n.6G>A
  variant of: http://identifiers.org/hgnc/17882
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000153914
  ensembl protein: ENSP00000428970
  ensembl transcript: ENST00000520953
  gene symbol: SREK1
  hgvsc: ENST00000520953.1:c.-36G>A
  variant of: http://identifiers.org/hgnc/17882
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1456
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24434
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 933
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5616
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18705
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

10-5242186-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242186
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242186
    reference: chr 10
allele count: 18
allele frequency: 1.48558977914232e-4
allele num: 121164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2241C>T
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.127G>A
  hgvsp: ENSP00000263126.1:p.Glu43Lys
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.127G>A
  hgvsp: ENSP00000369814.1:p.Glu43Lys
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2696
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5922
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6575
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42811
  bin: 9.75e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 1935
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1950
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1158
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu43Lys
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

10-5242192-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242192
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242192
    reference: chr 10
allele count: 1
allele frequency: 8.248511143738554e-6
allele num: 121234
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.133G>A
  hgvsp: ENSP00000369814.1:p.Gly45Ser
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2235C>T
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.133G>A
  hgvsp: ENSP00000263126.1:p.Gly45Ser
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5688
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5431
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5922
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1940
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42810
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1416
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly45Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

10-5242198-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242198
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242198
    reference: chr 10
allele count: 2
allele frequency: 1.649212501030758e-5
allele num: 121270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2229G>A
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.139C>T
  hgvsp: ENSP00000263126.1:p.Arg47Cys
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.139C>T
  hgvsp: ENSP00000369814.1:p.Arg47Cys
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4849
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5688
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5921
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2694
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1950
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1944
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 2170
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 1162
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genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42812
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Arg47Cys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

10-5242199-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242199
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242199
    reference: chr 10
allele count: 1
allele frequency: 8.246198502490351e-6
allele num: 121268
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2228C>T
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.140G>A
  hgvsp: ENSP00000263126.1:p.Arg47His
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.140G>A
  hgvsp: ENSP00000369814.1:p.Arg47His
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4850
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3821
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5921
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2691
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1945
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1162
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42811
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2170
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6704
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1950
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg47His
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

10-5242203-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242203
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242203
    reference: chr 10
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.144T>C
  hgvsp: ENST00000380448.1:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2224A>G
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.144T>C
  hgvsp: ENST00000263126.1:c.144T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5442
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5921
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1948
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6737
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42812
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1950
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 7.25e1
  variant carriers: 0
hgvs: p.His48His
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

10-5242204-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242204
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242204
    reference: chr 10
allele count: 3
allele frequency: 2.473288484368817e-5
allele num: 121296
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.145A>G
  hgvsp: ENSP00000369814.1:p.Ile49Val
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2223T>C
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.145A>G
  hgvsp: ENSP00000263126.1:p.Ile49Val
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5689
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5923
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6743
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42814
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1950
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1947
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile49Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

10-5242220-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242220
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242220
    reference: chr 10
allele count: 1
allele frequency: 8.242528148233626e-6
allele num: 121322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2207A>G
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.161T>C
  hgvsp: ENSP00000369814.1:p.Leu54Ser
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.161T>C
  hgvsp: ENSP00000263126.1:p.Leu54Ser
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5463
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5922
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5688
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6772
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42815
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1952
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu54Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

10-5242222-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242222
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242222
    reference: chr 10
allele count: 2
allele frequency: 1.648532805802836e-5
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.163T>A
  hgvsp: ENSP00000369814.1:p.Tyr55Asn
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2205A>T
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.163T>A
  hgvsp: ENSP00000263126.1:p.Tyr55Asn
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5688
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5925
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42815
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1952
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Tyr55Asn
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

10-5242222-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242222
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242222
    reference: chr 10
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2205A>G
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.163T>C
  hgvsp: ENSP00000263126.1:p.Tyr55His
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.163T>C
  hgvsp: ENSP00000369814.1:p.Tyr55His
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5925
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2578
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5688
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1413
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1952
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6774
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42815
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Tyr55His
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum

10-5242224-CAAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242224
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242221
    reference: chr 10
allele count: 40
allele frequency: 3.296956908773202e-4
allele num: 121324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.169_171delAAT
  hgvsp: ENSP00000263126.1:p.Asn57del
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.169_171delAAT
  hgvsp: ENSP00000369814.1:p.Asn57del
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2200_23+2202delATT
  variant of: http://identifiers.org/hgnc/23469
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5052
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5945
  bin: 9.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 6772
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42826
  bin: 9.75e1
  variant carriers: 40
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1950
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2168
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asn57del
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: CAAT
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

10-5242226-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242226
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242226
    reference: chr 10
allele count: 2
allele frequency: 1.649022129876983e-5
allele num: 121284
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.167A>G
  hgvsp: ENSP00000263126.1:p.Asn56Ser
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2201T>C
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.167A>G
  hgvsp: ENSP00000369814.1:p.Asn56Ser
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5458
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5931
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1948
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6777
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42804
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2167
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1952
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asn56Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

10-5242227-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242227
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242227
    reference: chr 10
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.168T>C
  hgvsp: ENST00000380448.1:c.168T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.168T>C
  hgvsp: ENST00000263126.1:c.168T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2200A>G
  variant of: http://identifiers.org/hgnc/23469
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5934
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42809
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1950
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6781
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1948
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asn56Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

10-5242227-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242227
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242227
    reference: chr 10
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.168T>G
  hgvsp: ENSP00000263126.1:p.Asn56Lys
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2200A>C
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.168T>G
  hgvsp: ENSP00000369814.1:p.Asn56Lys
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2693
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5934
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6781
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1948
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42809
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2167
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1950
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asn56Lys
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

10-5242231-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242231
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242231
    reference: chr 10
allele count: 2
allele frequency: 1.648505629646725e-5
allele num: 121322
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.172G>A
  hgvsp: ENSP00000369814.1:p.Glu58Lys
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.172G>A
  hgvsp: ENSP00000263126.1:p.Glu58Lys
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2196C>T
  variant of: http://identifiers.org/hgnc/23469
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5934
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6775
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42827
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1954
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2167
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu58Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

10-5242234-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242234
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242234
    reference: chr 10
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.175G>A
  hgvsp: ENSP00000263126.1:p.Glu59Lys
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2193C>T
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.175G>A
  hgvsp: ENSP00000369814.1:p.Glu59Lys
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5449
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2046
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5934
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42828
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6772
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1952
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1162
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2169
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1947
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu59Lys
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

10-5242243-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242243
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242243
    reference: chr 10
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.184G>A
  hgvsp: ENSP00000263126.1:p.Gly62Arg
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2184C>T
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.184G>A
  hgvsp: ENSP00000369814.1:p.Gly62Arg
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5933
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2046
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5448
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42828
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2166
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1954
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1945
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6771
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly62Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum

10-5242246-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242246
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242246
    reference: chr 10
allele count: 1
allele frequency: 8.24334350012365e-6
allele num: 121310
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2181G>A
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.187C>T
  hgvsp: ENST00000380448.1:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.187C>T
  hgvsp: ENST00000263126.1:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5416
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5686
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2046
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5933
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1956
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1947
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6746
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42828
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2166
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1162
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu63Leu
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

10-5242247-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242247
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242247
    reference: chr 10
allele count: 20
allele frequency: 1.648750247312537e-4
allele num: 121304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.188T>A
  hgvsp: ENSP00000263126.1:p.Leu63Gln
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2180A>T
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.188T>A
  hgvsp: ENSP00000369814.1:p.Leu63Gln
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5948
  bin: 9.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42833
  bin: 9.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1946
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1955
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6748
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu63Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

10-5242252-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242252
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242252
    reference: chr 10
allele count: 12
allele frequency: 9.894132779261898e-5
allele num: 121284
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.193A>G
  hgvsp: ENSP00000369814.1:p.Ile65Val
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.193A>G
  hgvsp: ENSP00000263126.1:p.Ile65Val
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2175T>C
  variant of: http://identifiers.org/hgnc/23469
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2702
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1954
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2163
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6701
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1945
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42838
  bin: 9.75e1
  variant carriers: 12
hgvs: p.Ile65Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

10-5242253-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242253
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242253
    reference: chr 10
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.194T>C
  hgvsp: ENSP00000369814.1:p.Ile65Thr
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.194T>C
  hgvsp: ENSP00000263126.1:p.Ile65Thr
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2174A>G
  variant of: http://identifiers.org/hgnc/23469
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2702
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5082
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4848
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1956
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1946
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42836
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6709
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2163
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile65Thr
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

10-5242255-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242255
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242255
    reference: chr 10
allele count: 6
allele frequency: 4.947719101494211e-5
allele num: 121268
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.196C>T
  hgvsp: ENSP00000369814.1:p.Arg66Ter
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2172G>A
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.196C>T
  hgvsp: ENSP00000263126.1:p.Arg66Ter
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2702
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5950
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2162
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1156
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42837
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 6683
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1951
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg66Ter
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS

10-5242256-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242256
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242256
    reference: chr 10
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.197G>T
  hgvsp: ENSP00000263126.1:p.Arg66Leu
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.197G>T
  hgvsp: ENSP00000369814.1:p.Arg66Leu
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2171C>A
  variant of: http://identifiers.org/hgnc/23469
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5330
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5949
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42837
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2162
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1951
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6679
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1157
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg66Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: African
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

10-5242260-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242260
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242260
    reference: chr 10
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2167G>C
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.201C>G
  hgvsp: ENSP00000369814.1:p.Ser67Arg
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.201C>G
  hgvsp: ENSP00000263126.1:p.Ser67Arg
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5264
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5950
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2161
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42837
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1949
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1153
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6612
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1947
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser67Arg
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

10-5242265-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242265
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242265
    reference: chr 10
allele count: 7
allele frequency: 5.780346820809248e-5
allele num: 121100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2162A>G
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.206T>C
  hgvsp: ENSP00000263126.1:p.Ile69Thr
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.206T>C
  hgvsp: ENSP00000369814.1:p.Ile69Thr
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4847
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5950
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5687
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1153
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42842
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1944
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6465
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2161
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile69Thr
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

10-5242266-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242266
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242266
    reference: chr 10
allele count: 1
allele frequency: 8.259411599517651e-6
allele num: 121074
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2161A>G
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.207T>C
  hgvsp: ENST00000380448.1:c.207T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.207T>C
  hgvsp: ENST00000263126.1:c.207T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5950
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5684
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5451
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2474
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42837
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1941
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1153
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6412
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2161
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile69Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/10-5242268-C-CA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242268
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242269
    reference: chr 10
allele count: 1
allele frequency: 8.266375690242371e-6
allele num: 120972
alternate allele: CA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.210dupA
  hgvsp: ENSP00000263126.1:p.Asp71ArgfsTer42
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2158dupT
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.210dupA
  hgvsp: ENSP00000369814.1:p.Asp71ArgfsTer42
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5692
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5950
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6267
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1920
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42838
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1945
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2160
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp71ArgfsTer42
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

10-5242270-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242270
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242270
    reference: chr 10
allele count: 1
allele frequency: 8.270067318347971e-6
allele num: 120918
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2157C>T
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.211G>A
  hgvsp: ENSP00000263126.1:p.Asp71Asn
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.211G>A
  hgvsp: ENSP00000369814.1:p.Asp71Asn
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5013
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5950
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1149
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42838
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6161
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1918
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2159
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1943
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp71Asn
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

10-5242272-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242272
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242272
    reference: chr 10
allele count: 1
allele frequency: 8.275131574592036e-6
allele num: 120844
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.213T>C
  hgvsp: ENST00000263126.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2155A>G
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.213T>C
  hgvsp: ENST00000380448.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5443
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5950
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4988
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2159
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6007
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42839
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1943
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1918
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Asp71Asp
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

10-5242277-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242277
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242277
    reference: chr 10
allele count: 4
allele frequency: 3.316914606033468e-5
allele num: 120594
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.218G>A
  hgvsp: ENSP00000369814.1:p.Ser73Asn
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.218G>A
  hgvsp: ENSP00000263126.1:p.Ser73Asn
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2150C>T
  variant of: http://identifiers.org/hgnc/23469
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5681
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5954
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5409
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2157
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1939
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5593
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1863
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 805
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser73Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

10-5242278-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242278
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242278
    reference: chr 10
allele count: 1
allele frequency: 8.296414289743973e-6
allele num: 120534
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.219T>C
  hgvsp: ENST00000263126.1:c.219T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2149A>G
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.219T>C
  hgvsp: ENST00000380448.1:c.219T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5952
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 874
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1853
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5478
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2157
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1940
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42840
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser73Ser
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

10-5242281-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242281
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242281
    reference: chr 10
allele count: 1
allele frequency: 8.311861025683651e-6
allele num: 120310
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.222G>C
  hgvsp: ENST00000380448.1:c.222G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.222G>C
  hgvsp: ENST00000263126.1:c.222G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2146C>G
  variant of: http://identifiers.org/hgnc/23469
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4083
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5952
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4696
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1792
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1138
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42840
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4795
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2157
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val74Val
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

10-5242286-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242286
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242286
    reference: chr 10
allele count: 2
allele frequency: 1.663948883490299e-5
allele num: 120196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.227G>A
  hgvsp: ENSP00000263126.1:p.Arg76Lys
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.227G>A
  hgvsp: ENSP00000369814.1:p.Arg76Lys
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2141C>T
  variant of: http://identifiers.org/hgnc/23469
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5618
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5293
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2156
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4682
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42840
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg76Lys
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-5242286-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242286
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242286
    reference: chr 10
allele count: 32
allele frequency: 2.662318213584479e-4
allele num: 120196
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.227G>C
  hgvsp: ENSP00000369814.1:p.Arg76Thr
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2141C>G
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.227G>C
  hgvsp: ENSP00000263126.1:p.Arg76Thr
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5293
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5961
  bin: 9.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1769
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2579
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4577
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2156
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1934
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1136
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4682
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg76Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

10-5242287-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242287
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242287
    reference: chr 10
allele count: 1
allele frequency: 8.320159747067144e-6
allele num: 120190
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.228A>G
  hgvsp: ENST00000380448.1:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.228A>G
  hgvsp: ENST00000263126.1:c.228A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2140T>C
  variant of: http://identifiers.org/hgnc/23469
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5949
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5271
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4595
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2156
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42839
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1353
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1933
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1134
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1780
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg76Arg
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-5242291-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242291
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242291
    reference: chr 10
allele count: 1
allele frequency: 8.331944675887353e-6
allele num: 120020
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.232G>A
  hgvsp: ENSP00000263126.1:p.Asp78Asn
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.232G>A
  hgvsp: ENSP00000369814.1:p.Asp78Asn
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2136C>T
  variant of: http://identifiers.org/hgnc/23469
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5949
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1933
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2156
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42840
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4276
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1763
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Asp78Asn
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

10-5242291-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242291
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242291
    reference: chr 10
allele count: 1
allele frequency: 8.331944675887353e-6
allele num: 120020
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.232G>T
  hgvsp: ENSP00000263126.1:p.Asp78Tyr
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.232G>T
  hgvsp: ENSP00000369814.1:p.Asp78Tyr
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2136C>A
  variant of: http://identifiers.org/hgnc/23469
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2051
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5949
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4276
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2156
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1129
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1933
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1763
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42840
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asp78Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

10-5242297-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242297
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242297
    reference: chr 10
allele count: 1
allele frequency: 8.34752412434472e-6
allele num: 119796
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.238T>G
  hgvsp: ENSP00000263126.1:p.Phe80Val
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2130A>C
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.238T>G
  hgvsp: ENSP00000369814.1:p.Phe80Val
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5948
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3323
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2155
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3600
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1924
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1119
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1928
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42839
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1691
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Phe80Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

10-5242300-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242300
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242300
    reference: chr 10
allele count: 1
allele frequency: 8.353939717970996e-6
allele num: 119704
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2127A>G
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.241T>C
  hgvsp: ENSP00000369814.1:p.Tyr81His
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.241T>C
  hgvsp: ENSP00000263126.1:p.Tyr81His
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5193
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5948
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5672
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1922
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
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genotype quality: GenotypeQuality
  all individuals: 1678
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 2154
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42840
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2025
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3490
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 508
  bin: 2.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1118
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genotype quality: GenotypeQuality
  all individuals: 493
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genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Tyr81His
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

10-5242301-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242301
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242301
    reference: chr 10
allele count: 1
allele frequency: 8.355475342992263e-6
allele num: 119682
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2126T>C
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.242A>G
  hgvsp: ENSP00000263126.1:p.Tyr81Cys
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.242A>G
  hgvsp: ENSP00000369814.1:p.Tyr81Cys
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5672
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3218
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5949
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1116
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2063
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2153
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3418
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1925
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1673
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 516
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Tyr81Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

10-5242310-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242310
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242310
    reference: chr 10
allele count: 2
allele frequency: 1.674901599531028e-5
allele num: 119410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.251A>G
  hgvsp: ENSP00000263126.1:p.Lys84Arg
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2117T>C
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.251A>G
  hgvsp: ENSP00000369814.1:p.Lys84Arg
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2865
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5948
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2582
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2964
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1112
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1918
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1409
  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 614
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42842
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1631
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2346
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2153
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys84Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: Latino
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

10-5242312-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 5242312
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 5242312
    reference: chr 10
allele count: 1
allele frequency: 8.379701012267883e-6
allele num: 119336
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000196326
  ensembl protein: ENSP00000394055
  ensembl transcript: ENST00000445191
  gene symbol: AKR1CL1
  hgvsc: ENST00000445191.1:c.23+2115C>G
  variant of: http://identifiers.org/hgnc/23469
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000263126
  ensembl transcript: ENST00000263126
  gene symbol: AKR1C4
  hgvsc: ENST00000263126.1:c.252+1G>C
  variant of: http://identifiers.org/hgnc/387
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000198610
  ensembl protein: ENSP00000369814
  ensembl transcript: ENST00000380448
  gene symbol: AKR1C4
  hgvsc: ENST00000380448.1:c.252+1G>C
  variant of: http://identifiers.org/hgnc/387
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5949
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2473
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5670
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2706
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2052
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1495
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2374
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1110
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2947
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42841
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 3.75e1
  variant carriers: 0
hgvs: c.252+1G>C
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 96
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3444
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1661
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 39912
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 108
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2128
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 68
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1532
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1162
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 924
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3888
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45029
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4944
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 608
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66112
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.719916288803627e-5
allele num: 11468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

African
type: Population
allele count: 14
allele frequency: 1.398601398601399e-3
allele num: 10010
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.48e-1

DP
type: SiteQuality
SIO_000300: 1.614646e6

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

QD
type: SiteQuality
SIO_000300: 1.41e1

FS
type: SiteQuality
SIO_000300: 4.202e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeDepth
all individuals: 39119
bin: 2.25e1
variant carriers: 53

GenotypeDepth
all individuals: 370
bin: 6.75e1
variant carriers: 114

GenotypeDepth
all individuals: 331
bin: 7.75e1
variant carriers: 117

GenotypeDepth
all individuals: 305
bin: 8.75e1
variant carriers: 125

GenotypeDepth
all individuals: 331
bin: 7.25e1
variant carriers: 124

GenotypeDepth
all individuals: 265
bin: 9.25e1
variant carriers: 96

GenotypeQuality
all individuals: 222
bin: 2.75e1
variant carriers: 64

GenotypeQuality
all individuals: 653
bin: 2.25e1
variant carriers: 64

GenotypeQuality
all individuals: 206
bin: 3.25e1
variant carriers: 62

GenotypeQuality
all individuals: 204
bin: 7.5e0
variant carriers: 42

GenotypeQuality
all individuals: 1337
bin: 7.75e1
variant carriers: 47

GenotypeQuality
all individuals: 854
bin: 2.5e0
variant carriers: 41

GenotypeQuality
all individuals: 165
bin: 5.75e1
variant carriers: 46

GenotypeQuality
all individuals: 199
bin: 1.75e1
variant carriers: 58

GenotypeQuality
all individuals: 191
bin: 4.25e1
variant carriers: 67

GenotypeQuality
all individuals: 200
bin: 3.75e1
variant carriers: 56

GenotypeQuality
all individuals: 1079
bin: 7.25e1
variant carriers: 49

GenotypeQuality
all individuals: 3615
bin: 6.75e1
variant carriers: 44

GenotypeQuality
all individuals: 188
bin: 1.25e1
variant carriers: 59

GenotypeQuality
all individuals: 1019
bin: 8.25e1
variant carriers: 51

GenotypeQuality
all individuals: 190
bin: 5.25e1
variant carriers: 55

GenotypeQuality
all individuals: 44152
bin: 6.25e1
variant carriers: 50

GenotypeQuality
all individuals: 188
bin: 4.75e1
variant carriers: 59

GenotypeQuality
all individuals: 762
bin: 9.25e1
variant carriers: 40

GenotypeQuality
all individuals: 523
bin: 8.75e1
variant carriers: 30

GenotypeQuality
all individuals: 4756
bin: 9.75e1
variant carriers: 856

European (Non-Finnish)
type: Population
allele count: 954
allele frequency: 1.474588846296525e-2
allele num: 64696
num of homozygotes: 0

Other
type: Population
allele count: 21
allele frequency: 2.436194895591647e-2
allele num: 862
num of homozygotes: 0

African
type: Population
allele count: 345
allele frequency: 3.622427551448971e-2
allele num: 9524
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.038774766014343e-4
allele num: 16454
num of homozygotes: 0

Latino
type: Population
allele count: 29
allele frequency: 2.537182852143482e-3
allele num: 11430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 257
allele frequency: 4.177503250975292e-2
allele num: 6152
num of homozygotes: 0

East Asian
type: Population
allele count: 28
allele frequency: 3.281762775433661e-3
allele num: 8532
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.267e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e0

MQRankSum
type: SiteQuality
SIO_000300: -4.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.402e0

DP
type: SiteQuality
SIO_000300: 1.741261e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.18e-2

FS
type: SiteQuality
SIO_000300: 4.9302e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.373e0

QD
type: SiteQuality
SIO_000300: 1.62e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

GenotypeDepth
all individuals: 418
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 535
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 192
bin: 7.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 340
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3419
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 114
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1153
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 907
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 101
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45157
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5008
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 586
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3969
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 490
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1512
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.52114390021296e-4
allele num: 6574
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508159140952553e-5
allele num: 66306
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.42e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.442e0

FS
type: SiteQuality
SIO_000300: 2.1622e1

DP
type: SiteQuality
SIO_000300: 1.647798e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.589e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

MQ
type: SiteQuality
SIO_000300: 5.92e1

MQRankSum
type: SiteQuality
SIO_000300: -3.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.72e-1

QD
type: SiteQuality
SIO_000300: 1.49e0

GenotypeDepth
all individuals: 8864
bin: 2.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 1669
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 219
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 531
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1156
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4006
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 379
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 906
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 589
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5009
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1512
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45593
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66426
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159017153453871e-4
allele num: 8628
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.887e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.22e0

QD
type: SiteQuality
SIO_000300: 1.21e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.97e-1

DP
type: SiteQuality
SIO_000300: 1.651502e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.54e-1

GenotypeDepth
all individuals: 813
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 8893
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1668
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 191
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 257
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 194
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 82
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1162
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 364
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5008
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 52
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1512
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1153
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4005
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45568
bin: 6.25e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.251e0

QD
type: SiteQuality
SIO_000300: 1.281e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.314e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 4.851e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.07e-1

DP
type: SiteQuality
SIO_000300: 1.652258e6

VQSLOD
type: SiteQuality
SIO_000300: 1.49e-1

GenotypeDepth
all individuals: 1667
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 123
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1230
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3421
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 256
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 535
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 587
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1153
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1514
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45615
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5007
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4009
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1164
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505162708088744e-5
allele num: 66438
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10212
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.4e-2

QD
type: SiteQuality
SIO_000300: 1.278e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 1.0364e1

DP
type: SiteQuality
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MQRankSum
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SIO_000300: -1.87e-1

InbreedingCoeff
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SIO_000300: 7.6e-3

VQSLOD
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SIO_000300: -7.307e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

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

Latino
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allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50407604608489e-5
allele num: 66486
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

MQ
type: SiteQuality
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FS
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ClippingRankSum
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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QD
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VQSLOD
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DP
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SIO_000300: 1.653894e6

InbreedingCoeff
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SIO_000300: 8.6e-3

GenotypeDepth
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.504030802550836e-5
allele num: 66488
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

FS
type: SiteQuality
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DP
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QD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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SIO_000300: 5.939e1

BaseQRankSum
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SIO_000300: -3.888e0

ClippingRankSum
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SIO_000300: -1.404e0

VQSLOD
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SIO_000300: -3.027e-1

GenotypeDepth
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variant carriers: 0

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

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

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

Other
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allele count: 0
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: 66480
num of homozygotes: 0

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

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

Latino
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allele frequency: 8.667013347200555e-5
allele num: 11538
num of homozygotes: 0

QD
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
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SIO_000300: 9.379999999999999e-1

FS
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InbreedingCoeff
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VQSLOD
type: SiteQuality
SIO_000300: 5.4e-2

BaseQRankSum
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SIO_000300: 4.62e-1

ReadPosRankSum
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SIO_000300: 4.96e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66464
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele num: 16482
num of homozygotes: 0

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

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

Latino
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num of homozygotes: 0

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

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

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

East Asian
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num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6586
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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -1.63e-1

MQRankSum
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SIO_000300: 1.91e0

BaseQRankSum
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SIO_000300: 3.13e0

MQ
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QD
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FS
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DP
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ClippingRankSum
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SIO_000300: -1.159e0

ReadPosRankSum
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SIO_000300: 1.04e0

InbreedingCoeff
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SIO_000300: -2.0e-4

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

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

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

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

Latino
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allele frequency: 8.706251088281386e-5
allele num: 11486
num of homozygotes: 0

East Asian
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DP
type: SiteQuality
SIO_000300: 1.642919e6

MQ
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VQSLOD
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FS
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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QD
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ClippingRankSum
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SIO_000300: -7.7e-2

ReadPosRankSum
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SIO_000300: -2.694e0

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

East Asian
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allele count: 0
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allele num: 8490
num of homozygotes: 0

African
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allele num: 9994
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 6
allele frequency: 9.204995244085791e-5
allele num: 65182
num of homozygotes: 0

South Asian
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FS
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SIO_000300: 0.0e0

DP
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QD
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SIO_000300: 1.149e1

InbreedingCoeff
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BaseQRankSum
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SIO_000300: 8.400000000000001e-2

ReadPosRankSum
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SIO_000300: 1.11e-1

VQSLOD
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MQ
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SIO_000300: 6.027e1

MQRankSum
type: SiteQuality
SIO_000300: 7.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-2

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65182
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16316
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Other
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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FS
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MQ
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VQSLOD
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MQRankSum
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QD
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BaseQRankSum
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SIO_000300: 8.400000000000001e-2

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16328
num of homozygotes: 0

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

African
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allele num: 9986
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65236
num of homozygotes: 0

Latino
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Other
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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DP
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FS
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ClippingRankSum
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VQSLOD
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QD
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BaseQRankSum
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SIO_000300: 2.37e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 1

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

African
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allele frequency: 1.004621257785815e-4
allele num: 9954
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
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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: 5
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allele num: 64964
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East Asian
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South Asian
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.49e-1

ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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VQSLOD
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MQ
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SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 6.75e-1

DP
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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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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6540
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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Other
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South Asian
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African
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allele count: 2
allele frequency: 2.010454362685967e-4
allele num: 9948
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European (Non-Finnish)
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allele count: 11
allele frequency: 1.694393099199014e-4
allele num: 64920
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MQRankSum
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MQ
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InbreedingCoeff
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QD
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VQSLOD
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FS
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DP
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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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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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 5000
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1135
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1405
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.085943527233452e-5
allele num: 64810
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9934
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.771929824561403e-5
allele num: 11400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16262
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8424
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.587046e6

MQRankSum
type: SiteQuality
SIO_000300: -1.8e-2

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.1e-2

QD
type: SiteQuality
SIO_000300: 1.402e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 2.082e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.649999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.55e0

GenotypeDepth
all individuals: 194
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 7.5e0
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GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 568
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GenotypeQuality
all individuals: 886
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9916
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.154603643525357e-5
allele num: 16248
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64666
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8386
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.26685393258427e-4
allele num: 11392
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.72e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-2

QD
type: SiteQuality
SIO_000300: 2.792e1

FS
type: SiteQuality
SIO_000300: 3.616e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

MQ
type: SiteQuality
SIO_000300: 5.979e1

DP
type: SiteQuality
SIO_000300: 1.57332e6

GenotypeQuality
all individuals: 436
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 178
bin: 4.75e1
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GenotypeQuality
all individuals: 182
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8954
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.619433198380567e-5
allele num: 61750
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8444
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11344
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
type: SiteQuality
SIO_000300: 1.87e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e-1

FS
type: SiteQuality
SIO_000300: 5.463e0

MQRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.371e1

DP
type: SiteQuality
SIO_000300: 1.49241e6

GenotypeQuality
all individuals: 2770
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3202
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7526
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variant carriers: 0

GenotypeQuality
all individuals: 98
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GenotypeQuality
all individuals: 1394
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 85
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GenotypeQuality
all individuals: 958
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variant carriers: 0

GenotypeQuality
all individuals: 886
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2220
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1077
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11318
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 9.157509157509158e-4
allele num: 9828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64210
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16184
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.4e0

MQ
type: SiteQuality
SIO_000300: 5.861e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.98e-1

DP
type: SiteQuality
SIO_000300: 1.52853e6

QD
type: SiteQuality
SIO_000300: 1.14e1

GenotypeQuality
all individuals: 446
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 569
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GenotypeQuality
all individuals: 3172
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variant carriers: 0

GenotypeQuality
all individuals: 1762
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GenotypeQuality
all individuals: 2496
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GenotypeQuality
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GenotypeQuality
all individuals: 407
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GenotypeQuality
all individuals: 291
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GenotypeQuality
all individuals: 102
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GenotypeQuality
all individuals: 7882
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variant carriers: 0

GenotypeQuality
all individuals: 84
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GenotypeQuality
all individuals: 504
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GenotypeQuality
all individuals: 1082
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GenotypeQuality
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GenotypeQuality
all individuals: 4994
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 100
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GenotypeQuality
all individuals: 30051
bin: 6.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 1.017501017501017e-4
allele num: 9828
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16192
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11304
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64200
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.754e0

MQ
type: SiteQuality
SIO_000300: 5.495e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 7.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.509e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.19e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -1.512e0

QD
type: SiteQuality
SIO_000300: 1.182e1

DP
type: SiteQuality
SIO_000300: 1.515176e6

GenotypeQuality
all individuals: 1001
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8861
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variant carriers: 0

GenotypeQuality
all individuals: 1311
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 487
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GenotypeQuality
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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: 886
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GenotypeQuality
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GenotypeQuality
all individuals: 1071
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GenotypeQuality
all individuals: 719
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GenotypeQuality
all individuals: 5000
bin: 9.75e1
variant carriers: 10

South Asian
type: Population
allele count: 11
allele frequency: 6.820436507936508e-4
allele num: 16128
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63812
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9744
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11276
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8266
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.69e-1

FS
type: SiteQuality
SIO_000300: 8.48e-1

DP
type: SiteQuality
SIO_000300: 1.474616e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

QD
type: SiteQuality
SIO_000300: 1.556e1

VQSLOD
type: SiteQuality
SIO_000300: 5.55e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 39

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3547
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variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63644
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.247191011235955e-3
allele num: 890
num of homozygotes: 0

South Asian
type: Population
allele count: 39
allele frequency: 2.421457841798088e-3
allele num: 16106
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9726
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11240
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.467606e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.09e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.13e-1

QD
type: SiteQuality
SIO_000300: 1.444e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e0

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 8.93e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9002
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4990
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variant carriers: 3

GenotypeQuality
all individuals: 565
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9684
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16108
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.725153567490944e-5
allele num: 63490
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11244
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.368e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.26e1

DP
type: SiteQuality
SIO_000300: 1.448082e6

VQSLOD
type: SiteQuality
SIO_000300: 5.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.52e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.25e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10992
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9364
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7954
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6426
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.250763929523438e-5
allele num: 61524
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.430385e6

VQSLOD
type: SiteQuality
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FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -5.73e-1

MQ
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -3.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.001e0

MQRankSum
type: SiteQuality
SIO_000300: 8.93e-1

QD
type: SiteQuality
SIO_000300: 3.382e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 15680
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59808
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10748
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7680
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.099868015838099e-4
allele num: 9092
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.855e1

MQRankSum
type: SiteQuality
SIO_000300: -9.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.824e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.36e-1

QD
type: SiteQuality
SIO_000300: 3.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-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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variant carriers: 1

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 7676
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 6426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 494
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African
type: Population
allele count: 1
allele frequency: 4.970178926441351e-4
allele num: 2012
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 166
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

QD
type: SiteQuality
SIO_000300: 1.433e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.879e0

VQSLOD
type: SiteQuality
SIO_000300: -2.034e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.93e-2

MQRankSum
type: SiteQuality
SIO_000300: -6.0e-3

FS
type: SiteQuality
SIO_000300: 4.576e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.8e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.49813e5

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7734
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6536
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 170
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 348
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2022
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
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MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.459e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.85e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

MQ
type: SiteQuality
SIO_000300: 5.705e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.02e0

QD
type: SiteQuality
SIO_000300: 7.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.22e-1

DP
type: SiteQuality
SIO_000300: 2.52545e5

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16394
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 8.648856428983279e-4
allele num: 10406
num of homozygotes: 0

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

Latino
type: Population
allele count: 8
allele frequency: 6.91085003455425e-4
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-1

FS
type: SiteQuality
SIO_000300: 1.771e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.641e1

QD
type: SiteQuality
SIO_000300: 2.53e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.93e-1

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.039e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.508e1

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

FS
type: SiteQuality
SIO_000300: 5.877e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-2

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.529e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-2

QD
type: SiteQuality
SIO_000300: 1.304e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.02e-1

DP
type: SiteQuality
SIO_000300: 3.377582e6

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.000210014701029e-5
allele num: 66662
num of homozygotes: 0

South Asian
type: Population
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Other
type: Population
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allele frequency: 0.0e0
allele num: 906
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

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

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

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e-1

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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VQSLOD
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DP
type: SiteQuality
SIO_000300: 3.378429e6

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
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: 66662
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Other
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allele num: 906
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East Asian
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African
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allele frequency: 0.0e0
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Latino
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South Asian
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DP
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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FS
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
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allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

East Asian
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Other
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allele frequency: 0.0e0
allele num: 906
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Latino
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African
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allele frequency: 0.0e0
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European (Finnish)
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66674
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 7.99e-1

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

African
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allele num: 10406
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East Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66674
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South Asian
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Other
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allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

East Asian
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South Asian
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European (Finnish)
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African
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Latino
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Other
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VQSLOD
type: SiteQuality
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InbreedingCoeff
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QD
type: SiteQuality
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DP
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SIO_000300: 3.379317e6

FS
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MQRankSum
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Latino
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allele num: 11576
num of homozygotes: 0

African
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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

European (Non-Finnish)
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allele count: 0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
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Other
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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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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
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MQRankSum
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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DP
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ReadPosRankSum
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QD
type: SiteQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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African
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Latino
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allele frequency: 0.0e0
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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QD
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VQSLOD
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DP
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FS
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BaseQRankSum
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

Latino
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allele frequency: 6.046993780234969e-4
allele num: 11576
num of homozygotes: 0

Other
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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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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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African
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allele frequency: 3.171247357293869e-3
allele num: 10406
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South Asian
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ClippingRankSum
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MQ
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DP
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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FS
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QD
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.6e-1

VQSLOD
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66680
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Other
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 1.728907330567082e-4
allele num: 11568
num of homozygotes: 0

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

African
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South Asian
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DP
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VQSLOD
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FS
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BaseQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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QD
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MQRankSum
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ClippingRankSum
type: SiteQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66680
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East Asian
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allele frequency: 1.158211721102618e-4
allele num: 8634
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European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11566
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African
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allele frequency: 0.0e0
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Other
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South Asian
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DP
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VQSLOD
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MQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

QD
type: SiteQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 8.646031471554557e-5
allele num: 11566
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African
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allele frequency: 0.0e0
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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BaseQRankSum
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QD
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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DP
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FS
type: SiteQuality
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ClippingRankSum
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MQ
type: SiteQuality
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499700059988002e-5
allele num: 66680
num of homozygotes: 0

Latino
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allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
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Other
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allele frequency: 0.0e0
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African
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
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ClippingRankSum
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FS
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DP
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QD
type: SiteQuality
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InbreedingCoeff
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MQ
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

African
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num of homozygotes: 0

Latino
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Other
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East Asian
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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 frequency: 1.499700059988002e-5
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num of homozygotes: 0

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

African
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East Asian
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European (Finnish)
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allele num: 6612
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South Asian
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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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European (Non-Finnish)
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allele frequency: 1.499700059988002e-5
allele num: 66680
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QD
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VQSLOD
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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FS
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DP
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ClippingRankSum
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Latino
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African
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Other
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele frequency: 1.499790029395885e-5
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East Asian
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QD
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BaseQRankSum
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ReadPosRankSum
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MQ
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FS
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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GenotypeQuality
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variant carriers: 0

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

Other
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European (Finnish)
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East Asian
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African
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allele frequency: 1.05708245243129e-3
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European (Non-Finnish)
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Latino
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South Asian
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MQ
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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FS
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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QD
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

European (Finnish)
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Latino
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allele frequency: 2.591568762957844e-4
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East Asian
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African
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European (Non-Finnish)
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allele frequency: 3.000030000300003e-5
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South Asian
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ReadPosRankSum
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BaseQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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QD
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MQRankSum
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DP
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SIO_000300: 3.382179e6

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 1947
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5001500150015e-5
allele num: 66660
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -6.53e-1

FS
type: SiteQuality
SIO_000300: 1.3856e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.83e-1

DP
type: SiteQuality
SIO_000300: 3.38196e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

MQ
type: SiteQuality
SIO_000300: 4.09e1

VQSLOD
type: SiteQuality
SIO_000300: -3.357e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.3e-2

QD
type: SiteQuality
SIO_000300: 1.259e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.68e-1

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500285054160291e-5
allele num: 66654
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: 8640
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.81e-2

FS
type: SiteQuality
SIO_000300: 6.022e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.206e0

VQSLOD
type: SiteQuality
SIO_000300: -1.996e0

QD
type: SiteQuality
SIO_000300: 1.158e1

DP
type: SiteQuality
SIO_000300: 3.38152e6

MQRankSum
type: SiteQuality
SIO_000300: -6.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.24e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

MQ
type: SiteQuality
SIO_000300: 4.306e1

GenotypeQuality
all individuals: 1948
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16328
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.050609353424986e-4
allele num: 66628
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.2e-1

DP
type: SiteQuality
SIO_000300: 3.380058e6

MQRankSum
type: SiteQuality
SIO_000300: 3.48e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.142e0

MQ
type: SiteQuality
SIO_000300: 4.337e1

QD
type: SiteQuality
SIO_000300: 1.239e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.1e-1

GenotypeQuality
all individuals: 1948
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16308
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501005673801447e-5
allele num: 66622
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.023e0

QD
type: SiteQuality
SIO_000300: 1.222e1

MQRankSum
type: SiteQuality
SIO_000300: -5.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -4.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.499e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

DP
type: SiteQuality
SIO_000300: 3.379277e6

MQ
type: SiteQuality
SIO_000300: 4.662e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.3e-2

GenotypeQuality
all individuals: 1411
bin: 8.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.156877231867996e-5
allele num: 16242
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66588
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.031e0

VQSLOD
type: SiteQuality
SIO_000300: 1.4e0

QD
type: SiteQuality
SIO_000300: 1.572e1

MQ
type: SiteQuality
SIO_000300: 4.328e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.271e0

FS
type: SiteQuality
SIO_000300: 1.87e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.7e-1

DP
type: SiteQuality
SIO_000300: 3.378092e6

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501907422426482e-5
allele num: 66582
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16194
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.23e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.17e0

QD
type: SiteQuality
SIO_000300: 1.22e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.46e-1

MQ
type: SiteQuality
SIO_000300: 3.099e1

VQSLOD
type: SiteQuality
SIO_000300: -3.576e0

DP
type: SiteQuality
SIO_000300: 3.376297e6

GenotypeQuality
all individuals: 1150
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66560
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.261e0

QD
type: SiteQuality
SIO_000300: 1.119e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.08e-1

FS
type: SiteQuality
SIO_000300: 2.919e0

DP
type: SiteQuality
SIO_000300: 3.374798e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.57e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

MQ
type: SiteQuality
SIO_000300: 4.218e1

GenotypeQuality
all individuals: 42840
bin: 9.75e1
variant carriers: 4

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15982
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 3.844675124951942e-4
allele num: 10404
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66476
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.204e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.76e-1

FS
type: SiteQuality
SIO_000300: 1.746e0

DP
type: SiteQuality
SIO_000300: 3.369633e6

MQRankSum
type: SiteQuality
SIO_000300: -1.046e0

MQ
type: SiteQuality
SIO_000300: 4.353e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.817e0

VQSLOD
type: SiteQuality
SIO_000300: -1.132e0

GenotypeQuality
all individuals: 1411
bin: 8.75e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.269592476489028e-5
allele num: 15950
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66456
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.284e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.9e-3

QD
type: SiteQuality
SIO_000300: 1.173e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.28e-1

DP
type: SiteQuality
SIO_000300: 3.367945e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.685e0

VQSLOD
type: SiteQuality
SIO_000300: -2.39e0

MQRankSum
type: SiteQuality
SIO_000300: -2.264e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.56e-1

GenotypeQuality
all individuals: 1936
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.332320162107397e-5
allele num: 15792
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.362e1

DP
type: SiteQuality
SIO_000300: 3.361447e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.152e0

MQRankSum
type: SiteQuality
SIO_000300: -6.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.508e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 4.522e1

GenotypeQuality
all individuals: 1934
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66374
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.272912423625254e-4
allele num: 15712
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.35915e6

MQ
type: SiteQuality
SIO_000300: 4.429e1

MQRankSum
type: SiteQuality
SIO_000300: 4.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

QD
type: SiteQuality
SIO_000300: 1.217e1

VQSLOD
type: SiteQuality
SIO_000300: -1.08e0

FS
type: SiteQuality
SIO_000300: 1.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

GenotypeQuality
all individuals: 42840
bin: 9.75e1
variant carriers: 32

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.013228071232712e-5
allele num: 66374
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.458412588621823e-4
allele num: 11566
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15712
num of homozygotes: 0

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

African
type: Population
allele count: 25
allele frequency: 2.404308520869398e-3
allele num: 10398
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

FS
type: SiteQuality
SIO_000300: 1.11e0

VQSLOD
type: SiteQuality
SIO_000300: -1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

DP
type: SiteQuality
SIO_000300: 3.35915e6

MQ
type: SiteQuality
SIO_000300: 4.429e1

MQRankSum
type: SiteQuality
SIO_000300: 4.64e-1

QD
type: SiteQuality
SIO_000300: 1.217e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15704
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66376
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.087e0

FS
type: SiteQuality
SIO_000300: 2.359e0

DP
type: SiteQuality
SIO_000300: 3.356605e6

MQ
type: SiteQuality
SIO_000300: 4.294e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.34e0

QD
type: SiteQuality
SIO_000300: 1.237e1

MQRankSum
type: SiteQuality
SIO_000300: -8.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.06e0

GenotypeQuality
all individuals: 1410
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507886245061673e-5
allele num: 66318
num of homozygotes: 0

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

South Asian
type: Population
allele count: 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

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

QD
type: SiteQuality
SIO_000300: 1.264e1

MQRankSum
type: SiteQuality
SIO_000300: -3.02e-1

DP
type: SiteQuality
SIO_000300: 3.351737e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.642e0

FS
type: SiteQuality
SIO_000300: 4.539e0

VQSLOD
type: SiteQuality
SIO_000300: -1.043e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e-1

MQ
type: SiteQuality
SIO_000300: 4.525e1

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66318
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.409434687860531e-5
allele num: 15602
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.539e0

MQ
type: SiteQuality
SIO_000300: 4.525e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.642e0

MQRankSum
type: SiteQuality
SIO_000300: -3.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.264e1

VQSLOD
type: SiteQuality
SIO_000300: -1.043e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e-1

DP
type: SiteQuality
SIO_000300: 3.351737e6

GenotypeQuality
all individuals: 87
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66256
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.474168069403081e-5
allele num: 15446
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -1.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.38e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.9e-1

FS
type: SiteQuality
SIO_000300: 1.781e0

MQ
type: SiteQuality
SIO_000300: 4.53e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.692e0

DP
type: SiteQuality
SIO_000300: 3.343409e6

QD
type: SiteQuality
SIO_000300: 1.236e1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509844184080203e-5
allele num: 66232
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15378
num of homozygotes: 0

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.07e0

VQSLOD
type: SiteQuality
SIO_000300: -5.899e0

DP
type: SiteQuality
SIO_000300: 3.341199e6

MQRankSum
type: SiteQuality
SIO_000300: -5.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.42e-1

MQ
type: SiteQuality
SIO_000300: 4.93e1

FS
type: SiteQuality
SIO_000300: 6.545999999999999e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 5.4e-1

GenotypeQuality
all individuals: 42840
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15366
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510072181450273e-5
allele num: 66222
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.408e1

VQSLOD
type: SiteQuality
SIO_000300: -1.219e0

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.45e0

DP
type: SiteQuality
SIO_000300: 3.340288e6

FS
type: SiteQuality
SIO_000300: 2.238e0

QD
type: SiteQuality
SIO_000300: 1.335e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
all individuals: 2373
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66144
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.318217769575534e-4
allele num: 15172
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.332986e6

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.71e-1

FS
type: SiteQuality
SIO_000300: 1.022e0

MQ
type: SiteQuality
SIO_000300: 5.24e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

QD
type: SiteQuality
SIO_000300: 1.285e1

VQSLOD
type: SiteQuality
SIO_000300: -9.159e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.05e-1