http://identifiers.org/exac.variant/6-33383810-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383810
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383810
    reference: chr 6
allele count: 1
allele frequency: 8.513246611727849e-6
allele num: 117464
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.919C>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.1639C>A
  hgvsp: ENST00000374516.3:c.1639C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000434347
  ensembl transcript: ENST00000495509
  gene symbol: PHF1
  hgvsc: ENST00000495509.2:c.*368C>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.654C>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*159C>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.481C>A
  hgvsp: ENST00000427826.1:c.481C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3369
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4248
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3157
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15860
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg547Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

6-33383810-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383810
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383810
    reference: chr 6
allele count: 1
allele frequency: 8.513246611727849e-6
allele num: 117464
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.1639C>T
  hgvsp: ENSP00000363640.3:p.Arg547Trp
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*159C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000434347
  ensembl transcript: ENST00000495509
  gene symbol: PHF1
  hgvsc: ENST00000495509.2:c.*368C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.481C>T
  hgvsp: ENSP00000404788.1:p.Arg161Trp
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.919C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.654C>T
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12403
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12857
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 239
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15860
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2139
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4248
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg547Trp
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD

6-33383820-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383820
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383820
    reference: chr 6
allele count: 1
allele frequency: 8.592098706029935e-6
allele num: 116386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*169G>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.1649G>A
  hgvsp: ENSP00000363640.3:p.Arg550Gln
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000434347
  ensembl transcript: ENST00000495509
  gene symbol: PHF1
  hgvsc: ENST00000495509.2:c.*378G>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.491G>A
  hgvsp: ENSP00000404788.1:p.Arg164Gln
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.929G>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.664G>A
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4206
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8885
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12062
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3837
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6769
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15513
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4751
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3050
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15340
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg550Gln
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

6-33383833-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383833
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383833
    reference: chr 6
allele count: 1
allele frequency: 8.694140149539211e-6
allele num: 115020
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.1662T>C
  hgvsp: ENST00000374516.3:c.1662T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.942T>C
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*182T>C
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.504T>C
  hgvsp: ENST00000427826.1:c.504T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.677T>C
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3292
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4205
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8882
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2140
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4243
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14772
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3038
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15514
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4379
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser554Ser
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: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

6-33383868-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383868
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383868
    reference: chr 6
allele count: 1
allele frequency: 9.084962569954213e-6
allele num: 110072
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.712T>C
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*217T>C
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.539T>C
  hgvsp: ENSP00000404788.1:p.Ile180Thr
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.1697T>C
  hgvsp: ENSP00000363640.3:p.Ile566Thr
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.977T>C
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6394
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2794
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4200
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12660
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1720
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3364
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3143
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13526
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4229
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2780
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15504
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile566Thr
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

6-33383869-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383869
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383869
    reference: chr 6
allele count: 1
allele frequency: 9.099015486524358e-6
allele num: 109902
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.978C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.540C>G
  hgvsp: ENSP00000404788.1:p.Ile180Met
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*218C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.1698C>G
  hgvsp: ENSP00000363640.3:p.Ile566Met
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.713C>G
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1721
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4200
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2757
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12659
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4733
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15503
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3365
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13523
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4230
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile566Met
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD

6-33383882-TGCCTCTGCCCA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383882
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383871
    reference: chr 6
allele count: 2
allele frequency: 1.838742300266618e-5
allele num: 108770
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: 3' UTR
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 11139
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12585
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1719
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2471
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4194
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2660
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8831
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3621
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2136
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2256
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6516
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4224
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4719
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2983
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13305
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: TGCCTCTGCCCA
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

6-33383896-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383896
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383896
    reference: chr 6
allele count: 10
allele frequency: 9.240948490953111e-5
allele num: 108214
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.*21T>C
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*245T>C
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.740T>C
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.1005T>C
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.*21T>C
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4174
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2652
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4065
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10876
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6354
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8780
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3355
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3865
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4204
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12834
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2119
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1858
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: East Asian
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

6-33383897-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383897
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383897
    reference: chr 6
allele count: 2
allele frequency: 1.848326340498679e-5
allele num: 108206
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.1006C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.*22C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*246C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.741C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.*22C>G
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6351
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4173
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8776
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12359
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 410
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3898
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 2965
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1867
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12832
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2118
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3355
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

6-33383899-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383899
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383899
    reference: chr 6
allele count: 1
allele frequency: 9.24658800902467e-6
allele num: 108148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.1008C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*248C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.*24C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.*24C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.743C>T
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8771
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4098
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12302
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2114
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12747
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3877
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4679
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2954
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3349
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

6-33383901-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383901
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383901
    reference: chr 6
allele count: 0
allele frequency: 0.0e0
allele num: 108074
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.*26A>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.*26A>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.1010A>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*250A>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.745A>G
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: 3' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8743
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4166
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
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genotype depth: GenotypeDepth
  all individuals: 12224
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genotype depth: GenotypeDepth
  all individuals: 179
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
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genotype depth: GenotypeDepth
  all individuals: 1708
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genotype quality: GenotypeQuality
  all individuals: 4181
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3835
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2110
  bin: 8.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2942
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 93
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6303
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

6-33383911-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383911
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383911
    reference: chr 6
allele count: 1
allele frequency: 9.27265309150254e-6
allele num: 107844
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.*36A>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.*36A>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.1020A>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*260A>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.755A>G
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10082
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2634
  bin: 5.25e1
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5923
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1664
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2095
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 882
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3606
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2863
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3338
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

6-33383913-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383913
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383913
    reference: chr 6
allele count: 1
allele frequency: 9.280397943463817e-6
allele num: 107754
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.1022C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.*38C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.757C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.*38C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*262C>G
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4137
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2830
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1664
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5792
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2090
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10988
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3326
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15424
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

6-33383913-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383913
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383913
    reference: chr 6
allele count: 1
allele frequency: 9.280397943463817e-6
allele num: 107754
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.*38C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.1022C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.757C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.*38C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*262C>T
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9889
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4137
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3326
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 706
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2830
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 449
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3532
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 662
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5792
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10988
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4564
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1664
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP

6-33383914-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383914
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383914
    reference: chr 6
allele count: 2
allele frequency: 1.856527550868855e-5
allele num: 107728
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*263G>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.758G>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.*39G>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.1023G>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.*39G>A
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6229
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8495
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 710
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2811
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1651
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3531
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4127
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10864
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3324
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2088
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

6-33383916-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383916
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383916
    reference: chr 6
allele count: 2
allele frequency: 1.857424124224525e-5
allele num: 107676
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.*41C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*265C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.1025C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.*41C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.760C>T
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10833
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1742
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2632
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2752
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1079
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3401
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4515
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1592
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4110
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10180
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15397
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff

6-33383918-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383918
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383918
    reference: chr 6
allele count: 2
allele frequency: 1.858977933931924e-5
allele num: 107586
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.*43C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*267C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.*43C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.762C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.1027C>G
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4086
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8919
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4106
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6172
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1577
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10446
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1149
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 799
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1258
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 949
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3247
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5290
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2705
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9066
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1488
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4488
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

6-33383919-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383919
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383919
    reference: chr 6
allele count: 1
allele frequency: 9.296272194849865e-6
allele num: 107570
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.763T>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.*44T>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*268T>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.1028T>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.*44T>A
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4105
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4191
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4090
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 937
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 725
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2074
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3265
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1260
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2704
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1499
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9203
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4098
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5279
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 808
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/6-33383922-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383922
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383922
    reference: chr 6
allele count: 1
allele frequency: 9.304922303898762e-6
allele num: 107470
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.*47C>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.*47C>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*271C>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.766C>A
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.1031C>A
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8262
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1420
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3130
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5097
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4471
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1057
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1353
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2072
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8037
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1822
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4092
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15392
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

6-33383922-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383922
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383922
    reference: chr 6
allele count: 1
allele frequency: 9.304922303898762e-6
allele num: 107470
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*271C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.*47C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.766C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.1031C>T
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.*47C>T
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2776
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6153
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8262
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4102
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1289
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8037
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1420
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1353
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5097
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2072
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15392
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4471
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1057
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3130
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

6-33383926-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33383926
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33383926
    reference: chr 6
allele count: 2
allele frequency: 1.862995323881737e-5
allele num: 107354
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000479029
  gene symbol: PHF1
  hgvsc: ENST00000479029.1:n.770C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000404788
  ensembl transcript: ENST00000427826
  gene symbol: PHF1
  hgvsc: ENST00000427826.1:c.*51C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363640
  ensembl transcript: ENST00000374516
  gene symbol: PHF1
  hgvsc: ENST00000374516.3:c.*51C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112511
  ensembl transcript: ENST00000486845
  gene symbol: PHF1
  hgvsc: ENST00000486845.1:n.1035C>G
  variant of: http://identifiers.org/hgnc/8919
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112511
  ensembl protein: ENSP00000363636
  ensembl transcript: ENST00000374512
  gene symbol: PHF1
  hgvsc: ENST00000374512.3:c.*275C>G
  variant of: http://identifiers.org/hgnc/8919
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6133
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9552
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4094
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1608
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1201
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 553
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4895
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2623
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1164
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 995
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2211
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 723
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2099
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15391
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6709
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2072
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum

6-33384352-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384352
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384352
    reference: chr 6
allele count: 1
allele frequency: 8.411277841329655e-6
allele num: 118888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.921C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*97C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*75C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*75C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.*50C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*576C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.937C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*298C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*75C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1364C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*75C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.529C>T
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9870
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1060
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5383
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

6-33384355-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384355
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384355
    reference: chr 6
allele count: 1
allele frequency: 8.410711882653748e-6
allele num: 118896
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.*47G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*72G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*72G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*72G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*295G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.918G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*573G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*72G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*94G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.934G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1361G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.526G>A
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5380
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

6-33384365-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384365
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384363
    reference: chr 6
allele count: 1
allele frequency: 8.39560070523046e-6
allele num: 119110
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*283_*284delCA
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.*35_*36delCA
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*60_*61delCA
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*82_*83delCA
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1349_1350delCA
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*60_*61delCA
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*60_*61delCA
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.906_907delCA
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.514_515delCA
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*60_*61delCA
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.922_923delCA
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*561_*562delCA
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5195
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2367
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7207
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: CTG
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

6-33384367-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384367
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384367
    reference: chr 6
allele count: 1
allele frequency: 8.387432271484408e-6
allele num: 119226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*60C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.*35C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*60C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*60C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*60C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*561C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1349C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*82C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.922C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*283C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.906C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.514C>T
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2255
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7213
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

6-33384374-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384374
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384374
    reference: chr 6
allele count: 13
allele frequency: 1.088467270626455e-4
allele num: 119434
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1342T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.*28T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*53T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.899T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.915T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*53T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*75T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*554T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*276T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*53T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.507T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*53T>C
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8632
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1924
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9783
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5374
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7207
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ

6-33384379-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384379
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384379
    reference: chr 6
allele count: 1
allele frequency: 8.361064196250898e-6
allele num: 119602
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.502C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.910C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*271C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1337C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.*23C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*48C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.894C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*70C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*549C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*48C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*48C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*48C>A
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5374
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3528
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

6-33384380-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384380
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384380
    reference: chr 6
allele count: 2
allele frequency: 1.673108132978634e-5
allele num: 119538
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*548G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*47G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.501G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*47G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*47G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*47G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.*22G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*69G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.893G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.909G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*270G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1336G>A
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

6-33384380-CGTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384380
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384377
    reference: chr 6
allele count: 1
allele frequency: 8.365540664893172e-6
allele num: 119538
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*44_*46delAAC
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.498_500delAAC
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.906_908delAAC
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.*19_*21delAAC
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*44_*46delAAC
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*44_*46delAAC
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1333_1335delAAC
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*267_*269delAAC
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*44_*46delAAC
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.890_892delAAC
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*66_*68delAAC
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*545_*547delAAC
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7208
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6370
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10089
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: CGTT
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

6-33384389-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384389
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384389
    reference: chr 6
allele count: 1
allele frequency: 8.334861391255063e-6
allele num: 119978
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*38T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.884T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*261T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*38T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*539T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*60T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.900T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.*13T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*38T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.492T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*38T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1327T>C
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10140
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5373
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3528
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD

6-33384390-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384390
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384390
    reference: chr 6
allele count: 6
allele frequency: 5.000166672222407e-5
allele num: 119996
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1326A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.*12A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*59A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*37A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*538A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.883A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*37A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*37A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*260A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.491A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.899A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*37A>G
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7211
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1390
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6968
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5374
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

6-33384392-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384392
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384392
    reference: chr 6
allele count: 1
allele frequency: 8.326671995736744e-6
allele num: 120096
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*35C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*57C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.897C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.*10C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*258C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*35C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*35C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*35C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.489C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*536C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.881C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1324C>T
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

6-33384392-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384392
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384392
    reference: chr 6
allele count: 1
allele frequency: 8.326671995736744e-6
allele num: 120096
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.489C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*35C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*35C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*35C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*536C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.*10C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*35C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*57C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.897C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*258C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.881C>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1324C>A
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 889
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

6-33384393-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384393
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384393
    reference: chr 6
allele count: 1
allele frequency: 8.326256015719971e-6
allele num: 120102
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*34G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*56G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.896G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*535G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*34G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*257G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1323G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*34G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*34G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.*9G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.880G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.488G>A
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10222
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: MQ

6-33384394-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384394
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384394
    reference: chr 6
allele count: 1
allele frequency: 8.31766839119658e-6
allele num: 120226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.879C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*534C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*55C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*33C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*33C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*256C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*33C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*33C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.895C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1322C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.*8C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.487C>T
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7215
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10414
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5376
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

6-33384409-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384409
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384409
    reference: chr 6
allele count: 1
allele frequency: 8.286651861182008e-6
allele num: 120676
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.880C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*40C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*241C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.401C>T
  hgvsp: ENSP00000418659.1:p.Ser134Leu
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*18C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.864C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*519C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*18C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1307C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.472C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*18C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*18C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.*18C>T
  variant of: http://identifiers.org/hgnc/21101
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7480
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8652
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser134Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

6-33384412-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384412
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384412
    reference: chr 6
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*516G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*15G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*15G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.398G>A
  hgvsp: ENSP00000418659.1:p.Cys133Tyr
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*15G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*238G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*15G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.*15G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.877G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1304G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.861G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*37G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.469G>A
  variant of: http://identifiers.org/hgnc/21101
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8657
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5380
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys133Tyr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

6-33384420-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384420
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384420
    reference: chr 6
allele count: 1
allele frequency: 8.273762245168123e-6
allele num: 120864
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1296C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*230C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*7C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*29C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.*7C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*7C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*7C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*7C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.390C>T
  hgvsp: ENST00000494751.1:c.390C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.853C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.869C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*508C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.461C>T
  variant of: http://identifiers.org/hgnc/21101
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10792
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro130Pro
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/6-33384423-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384423
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384423
    reference: chr 6
allele count: 2
allele frequency: 1.654232353476369e-5
allele num: 120902
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1293G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.387G>T
  hgvsp: ENSP00000418659.1:p.Glu129Asp
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.850G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*4G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*4G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*4G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*227G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.458G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*505G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*26G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.*4G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*4G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.866G>T
  variant of: http://identifiers.org/hgnc/21101
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu129Asp
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

6-33384423-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384423
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384423
    reference: chr 6
allele count: 1
allele frequency: 8.271161767381846e-6
allele num: 120902
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1293G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*4G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*4G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*227G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.850G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*26G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*4G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*4G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.387G>A
  hgvsp: ENST00000494751.1:c.387G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.*4G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.458G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*505G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.866G>A
  variant of: http://identifiers.org/hgnc/21101
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7227
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10367
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5378
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu129Glu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

6-33384424-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384424
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384424
    reference: chr 6
allele count: 1
allele frequency: 8.269656974628692e-6
allele num: 120924
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*504A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.*3A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.457A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1292A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.*3A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.*3A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.*3A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.*3A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.849A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*226A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.386A>G
  hgvsp: ENSP00000418659.1:p.Glu129Gly
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*25A>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.865A>G
  variant of: http://identifiers.org/hgnc/21101
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7519
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10365
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7224
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8658
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu129Gly
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/6-33384428-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384428
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384428
    reference: chr 6
allele count: 3
allele frequency: 2.47999470934462e-5
allele num: 120968
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.470G>T
  hgvsp: ENSP00000363620.3:p.Ter157LeuextTer1
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.845G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.470G>T
  hgvsp: ENSP00000403268.2:p.Ter157LeuextTer1
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.382G>T
  hgvsp: ENSP00000418659.1:p.Asp128Tyr
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: stop_lost
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.596G>T
  hgvsp: ENSP00000363624.5:p.Ter199LeuextTer1
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*500G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.539G>T
  hgvsp: ENSP00000417544.1:p.Ter180LeuextTer1
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.470G>T
  hgvsp: ENSP00000475963.1:p.Ter157LeuextTer1
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*222G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*21G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.861G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.453G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1288G>T
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7233
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter199LeuextTer1
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

6-33384428-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384428
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384428
    reference: chr 6
allele count: 7
allele frequency: 5.786654321804114e-5
allele num: 120968
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1288G>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.845G>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.861G>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*500G>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.539G>C
  hgvsp: ENSP00000417544.1:p.Ter180SerextTer1
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.470G>C
  hgvsp: ENSP00000475963.1:p.Ter157SerextTer1
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: stop_lost
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.596G>C
  hgvsp: ENSP00000363624.5:p.Ter199SerextTer1
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*21G>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.470G>C
  hgvsp: ENSP00000403268.2:p.Ter157SerextTer1
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*222G>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.470G>C
  hgvsp: ENSP00000363620.3:p.Ter157SerextTer1
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.453G>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.382G>C
  hgvsp: ENSP00000418659.1:p.Asp128His
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5381
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7520
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2275
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10831
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7233
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter199SerextTer1
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

6-33384429-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384429
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384429
    reference: chr 6
allele count: 1
allele frequency: 8.265282507356101e-6
allele num: 120988
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*221T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.452T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.469T>C
  hgvsp: ENSP00000403268.2:p.Ter157ArgextTer1
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.469T>C
  hgvsp: ENSP00000475963.1:p.Ter157ArgextTer1
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.538T>C
  hgvsp: ENSP00000417544.1:p.Ter180ArgextTer1
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: stop_lost
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.595T>C
  hgvsp: ENSP00000363624.5:p.Ter199ArgextTer1
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.469T>C
  hgvsp: ENSP00000363620.3:p.Ter157ArgextTer1
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*499T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*20T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.860T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1287T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.381T>C
  hgvsp: ENST00000494751.1:c.381T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.844T>C
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5382
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3534
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ter199ArgextTer1
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

6-33384432-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384432
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384431
    reference: chr 6
allele count: 1
allele frequency: 8.263643275047103e-6
allele num: 121012
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.840delG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.465delG
  hgvsp: ENSP00000403268.2:p.Pro156HisfsTer10
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.448delG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*217delG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.377delG
  hgvsp: ENSP00000418659.1:p.Cys126SerfsTer?
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*495delG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.465delG
  hgvsp: ENSP00000475963.1:p.Pro156HisfsTer10
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.856delG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.534delG
  hgvsp: ENSP00000417544.1:p.Pro179HisfsTer10
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1283delG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.465delG
  hgvsp: ENSP00000363620.3:p.Pro156HisfsTer10
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*16delG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.591delG
  hgvsp: ENSP00000363624.5:p.Pro198HisfsTer10
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7232
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5385
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 838
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro198HisfsTer10
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: GC
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/6-33384438-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384438
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384438
    reference: chr 6
allele count: 16
allele frequency: 1.321527686005022e-4
allele num: 121072
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*212G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.460G>T
  hgvsp: ENSP00000403268.2:p.Val154Phe
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.460G>T
  hgvsp: ENSP00000475963.1:p.Val154Phe
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.851G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1278G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.*11G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.373-1G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.460G>T
  hgvsp: ENSP00000363620.3:p.Val154Phe
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*490G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.529G>T
  hgvsp: ENSP00000417544.1:p.Val177Phe
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.586G>T
  hgvsp: ENSP00000363624.5:p.Val196Phe
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.835G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.443G>T
  variant of: http://identifiers.org/hgnc/21101
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7568
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8676
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7234
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5393
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10867
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: c.373-1G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

6-33384458-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384458
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384458
    reference: chr 6
allele count: 1
allele frequency: 8.249599894405122e-6
allele num: 121218
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*192C>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.831C>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*470C>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.509C>G
  hgvsp: ENSP00000417544.1:p.Ser170Ter
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.440C>G
  hgvsp: ENSP00000363620.3:p.Ser147Ter
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.440C>G
  hgvsp: ENSP00000403268.2:p.Ser147Ter
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.440C>G
  hgvsp: ENSP00000475963.1:p.Ser147Ter
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.566C>G
  hgvsp: ENSP00000363624.5:p.Ser189Ter
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.459C>G
  hgvsp: ENST00000488478.1:c.459C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.815C>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.373-21C>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1258C>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.423C>G
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5390
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10929
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser189Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

6-33384459-ACT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384459
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384457
    reference: chr 6
allele count: 1
allele frequency: 8.249327679794096e-6
allele num: 121222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.437_438delAG
  hgvsp: ENSP00000363620.3:p.Glu146ValfsTer4
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.828_829delAG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.506_507delAG
  hgvsp: ENSP00000417544.1:p.Glu169ValfsTer4
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.437_438delAG
  hgvsp: ENSP00000403268.2:p.Glu146ValfsTer4
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.456_457delAG
  hgvsp: ENSP00000418612.1:p.Arg152SerfsTer20
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.437_438delAG
  hgvsp: ENSP00000475963.1:p.Glu146ValfsTer4
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*467_*468delAG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.420_421delAG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*189_*190delAG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.563_564delAG
  hgvsp: ENSP00000363624.5:p.Glu188ValfsTer4
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.812_813delAG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1255_1256delAG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.373-24_373-23delAG
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10420
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10931
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu188ValfsTer4
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: ACT
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

6-33384461-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384461
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384461
    reference: chr 6
allele count: 1
allele frequency: 8.248239000973292e-6
allele num: 121238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.812A>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*189A>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.563A>T
  hgvsp: ENSP00000363624.5:p.Glu188Val
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.437A>T
  hgvsp: ENSP00000363620.3:p.Glu146Val
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.437A>T
  hgvsp: ENSP00000403268.2:p.Glu146Val
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.506A>T
  hgvsp: ENSP00000417544.1:p.Glu169Val
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.420A>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*467A>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1255A>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.456A>T
  hgvsp: ENSP00000418612.1:p.Arg152Ser
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.828A>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.373-24A>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.437A>T
  hgvsp: ENSP00000475963.1:p.Glu146Val
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10943
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu188Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum

6-33384461-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384461
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384461
    reference: chr 6
allele count: 3
allele frequency: 2.474471700291988e-5
allele num: 121238
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.420A>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.437A>C
  hgvsp: ENSP00000403268.2:p.Glu146Ala
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.506A>C
  hgvsp: ENSP00000417544.1:p.Glu169Ala
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1255A>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.373-24A>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*467A>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.812A>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.437A>C
  hgvsp: ENSP00000475963.1:p.Glu146Ala
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.563A>C
  hgvsp: ENSP00000363624.5:p.Glu188Ala
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.437A>C
  hgvsp: ENSP00000363620.3:p.Glu146Ala
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*189A>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.456A>C
  hgvsp: ENSP00000418612.1:p.Arg152Ser
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.828A>C
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7707
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu188Ala
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

6-33384462-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384462
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384460
    reference: chr 6
allele count: 6
allele frequency: 4.948616861587186e-5
allele num: 121246
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.503_504delCA
  hgvsp: ENSP00000417544.1:p.Thr168ArgfsTer5
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.825_826delCA
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.373-27_373-26delCA
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.434_435delCA
  hgvsp: ENSP00000475963.1:p.Thr145ArgfsTer5
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1252_1253delCA
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.560_561delCA
  hgvsp: ENSP00000363624.5:p.Thr187ArgfsTer5
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.809_810delCA
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.453_454delCA
  hgvsp: ENSP00000418612.1:p.His151GlnfsTer21
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.434_435delCA
  hgvsp: ENSP00000363620.3:p.Thr145ArgfsTer5
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*186_*187delCA
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.434_435delCA
  hgvsp: ENSP00000403268.2:p.Thr145ArgfsTer5
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.417_418delCA
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*464_*465delCA
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7238
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2279
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5388
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr187ArgfsTer5
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: CTG
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum

6-33384464-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384464
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384464
    reference: chr 6
allele count: 10
allele frequency: 8.24783082049421e-5
allele num: 121244
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.503C>G
  hgvsp: ENSP00000417544.1:p.Thr168Arg
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.825C>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.434C>G
  hgvsp: ENSP00000363620.3:p.Thr145Arg
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.453C>G
  hgvsp: ENSP00000418612.1:p.His151Gln
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.434C>G
  hgvsp: ENSP00000475963.1:p.Thr145Arg
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.560C>G
  hgvsp: ENSP00000363624.5:p.Thr187Arg
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.417C>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1252C>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.809C>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.434C>G
  hgvsp: ENSP00000403268.2:p.Thr145Arg
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*186C>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*464C>G
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.373-27C>G
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5387
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10416
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr187Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

6-33384468-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384468
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384468
    reference: chr 6
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.821G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*460G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.499G>A
  hgvsp: ENSP00000417544.1:p.Val167Ile
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.413G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.373-31G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.556G>A
  hgvsp: ENSP00000363624.5:p.Val186Ile
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.449G>A
  hgvsp: ENSP00000418612.1:p.Gly150Asp
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.430G>A
  hgvsp: ENSP00000403268.2:p.Val144Ile
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1248G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*182G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.430G>A
  hgvsp: ENSP00000363620.3:p.Val144Ile
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.430G>A
  hgvsp: ENSP00000475963.1:p.Val144Ile
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.805G>A
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8680
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val186Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

6-33384473-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384473
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384473
    reference: chr 6
allele count: 2465
allele frequency: 2.032453290677924e-2
allele num: 121282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*455G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.425G>A
  hgvsp: ENSP00000403268.2:p.Arg142His
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.816G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.800G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*177G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.494G>A
  hgvsp: ENSP00000417544.1:p.Arg165His
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.408G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.551G>A
  hgvsp: ENSP00000363624.5:p.Arg184His
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.425G>A
  hgvsp: ENSP00000475963.1:p.Arg142His
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.425G>A
  hgvsp: ENSP00000363620.3:p.Arg142His
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1243G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.444G>A
  hgvsp: ENST00000488478.1:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.373-36G>A
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8450
  bin: 3.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 5164
  bin: 4.75e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.75e1
  variant carriers: 223
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 9.25e1
  variant carriers: 149
genotype depth: GenotypeDepth
  all individuals: 7611
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10272
  bin: 3.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 8.25e1
  variant carriers: 167
genotype depth: GenotypeDepth
  all individuals: 3368
  bin: 5.25e1
  variant carriers: 140
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10832
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 7.25e1
  variant carriers: 214
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 6.75e1
  variant carriers: 255
genotype depth: GenotypeDepth
  all individuals: 7023
  bin: 4.25e1
  variant carriers: 79
genotype quality: GenotypeQuality
hgvs: p.Arg184His
num of homozygotes: 57
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

6-33384474-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384474
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384474
    reference: chr 6
allele count: 18
allele frequency: 1.484168865435356e-4
allele num: 121280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*176C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1242C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.407C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.424C>T
  hgvsp: ENSP00000363620.3:p.Arg142Cys
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.493C>T
  hgvsp: ENSP00000417544.1:p.Arg165Cys
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.443C>T
  hgvsp: ENSP00000418612.1:p.Ala148Val
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.799C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.550C>T
  hgvsp: ENSP00000363624.5:p.Arg184Cys
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.424C>T
  hgvsp: ENSP00000403268.2:p.Arg142Cys
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.424C>T
  hgvsp: ENSP00000475963.1:p.Arg142Cys
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.373-37C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*454C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.815C>T
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8740
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10680
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7244
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Arg184Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/6-33384477-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384477
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384477
    reference: chr 6
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.547G>T
  hgvsp: ENSP00000363624.5:p.Val183Leu
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1239G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*451G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*173G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.490G>T
  hgvsp: ENSP00000417544.1:p.Val164Leu
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.421G>T
  hgvsp: ENSP00000363620.3:p.Val141Leu
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.373-40G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.421G>T
  hgvsp: ENSP00000475963.1:p.Val141Leu
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.440G>T
  hgvsp: ENSP00000418612.1:p.Gly147Val
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.812G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.421G>T
  hgvsp: ENSP00000403268.2:p.Val141Leu
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.796G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.404G>T
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8742
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7244
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val183Leu
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

6-33384485-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384485
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384485
    reference: chr 6
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1231T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.413T>C
  hgvsp: ENSP00000363620.3:p.Leu138Pro
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.482T>C
  hgvsp: ENSP00000417544.1:p.Leu161Pro
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.413T>C
  hgvsp: ENSP00000475963.1:p.Leu138Pro
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.432T>C
  hgvsp: ENST00000488478.1:c.432T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.804T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.539T>C
  hgvsp: ENSP00000363624.5:p.Leu180Pro
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*443T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.413T>C
  hgvsp: ENSP00000403268.2:p.Leu138Pro
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.372+41T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.788T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.396T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*165T>C
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8743
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7247
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Leu180Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

6-33384490-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384490
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384490
    reference: chr 6
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.408G>C
  hgvsp: ENST00000374496.3:c.408G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*438G>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.799G>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.408G>C
  hgvsp: ENST00000607266.1:c.408G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.372+36G>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.783G>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.534G>C
  hgvsp: ENST00000374500.5:c.534G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*160G>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1226G>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.427G>C
  hgvsp: ENSP00000418612.1:p.Val143Leu
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.391G>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.477G>C
  hgvsp: ENST00000488034.1:c.477G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.408G>C
  hgvsp: ENST00000440279.3:c.408G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7247
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val143Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

6-33384490-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384490
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384490
    reference: chr 6
allele count: 2
allele frequency: 1.648315421639085e-5
allele num: 121336
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.534G>A
  hgvsp: ENST00000374500.5:c.534G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.408G>A
  hgvsp: ENST00000440279.3:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.783G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.799G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.372+36G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.477G>A
  hgvsp: ENST00000488034.1:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*160G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.427G>A
  hgvsp: ENSP00000418612.1:p.Val143Ile
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.391G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.408G>A
  hgvsp: ENST00000374496.3:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1226G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.408G>A
  hgvsp: ENST00000607266.1:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*438G>A
  variant of: http://identifiers.org/hgnc/21101
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8745
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val143Ile
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

6-33384491-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384491
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384491
    reference: chr 6
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.390C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.407C>T
  hgvsp: ENSP00000363620.3:p.Pro136Leu
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.782C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.476C>T
  hgvsp: ENSP00000417544.1:p.Pro159Leu
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*437C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.407C>T
  hgvsp: ENSP00000475963.1:p.Pro136Leu
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.372+35C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.798C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.407C>T
  hgvsp: ENSP00000403268.2:p.Pro136Leu
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.533C>T
  hgvsp: ENSP00000363624.5:p.Pro178Leu
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*159C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.426C>T
  hgvsp: ENST00000488478.1:c.426C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1225C>T
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7714
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11309
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro178Leu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

6-33384501-CCT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384501
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384499
    reference: chr 6
allele count: 2
allele frequency: 1.648070932972955e-5
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.395_396delAG
  hgvsp: ENSP00000403268.2:p.Gln132ArgfsTer18
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.414_415delAG
  hgvsp: ENSP00000418612.1:p.Glu140ThrfsTer32
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.372+23_372+24delAG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.464_465delAG
  hgvsp: ENSP00000417544.1:p.Gln155ArgfsTer18
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.521_522delAG
  hgvsp: ENSP00000363624.5:p.Gln174ArgfsTer18
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*425_*426delAG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1213_1214delAG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.770_771delAG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.395_396delAG
  hgvsp: ENSP00000475963.1:p.Gln132ArgfsTer18
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.395_396delAG
  hgvsp: ENSP00000363620.3:p.Gln132ArgfsTer18
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*147_*148delAG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.786_787delAG
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.378_379delAG
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8747
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Gln174ArgfsTer18
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: CCT
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

6-33384502-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384502
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384502
    reference: chr 6
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*426G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.372+24G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.396G>A
  hgvsp: ENST00000440279.3:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.787G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.465G>A
  hgvsp: ENST00000488034.1:c.465G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.396G>A
  hgvsp: ENST00000374496.3:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.415G>A
  hgvsp: ENSP00000418612.1:p.Gly139Arg
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.379G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*148G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.396G>A
  hgvsp: ENST00000607266.1:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.522G>A
  hgvsp: ENST00000374500.5:c.522G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1214G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.771G>A
  variant of: http://identifiers.org/hgnc/21101
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8743
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7711
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10698
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly139Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

6-33384504-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384504
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384504
    reference: chr 6
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.372+22C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.394C>T
  hgvsp: ENSP00000363620.3:p.Gln132Ter
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.463C>T
  hgvsp: ENSP00000417544.1:p.Gln155Ter
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.394C>T
  hgvsp: ENSP00000475963.1:p.Gln132Ter
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*146C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.413C>T
  hgvsp: ENSP00000418612.1:p.Thr138Ile
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1212C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.520C>T
  hgvsp: ENSP00000363624.5:p.Gln174Ter
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.785C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.394C>T
  hgvsp: ENSP00000403268.2:p.Gln132Ter
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.377C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*424C>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.769C>T
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1299
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10699
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln174Ter
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum

http://identifiers.org/exac.variant/6-33384514-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384514
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384514
    reference: chr 6
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.384G>T
  hgvsp: ENSP00000363620.3:p.Leu128Phe
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.775G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.372+12G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1202G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.759G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.510G>T
  hgvsp: ENSP00000363624.5:p.Leu170Phe
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.453G>T
  hgvsp: ENSP00000417544.1:p.Leu151Phe
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.403G>T
  hgvsp: ENSP00000418612.1:p.Ala135Ser
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.367G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*136G>T
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.384G>T
  hgvsp: ENSP00000475963.1:p.Leu128Phe
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.384G>T
  hgvsp: ENSP00000403268.2:p.Leu128Phe
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*414G>T
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7233
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu170Phe
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

6-33384514-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384514
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384514
    reference: chr 6
allele count: 5
allele frequency: 4.119905736556747e-5
allele num: 121362
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.384G>A
  hgvsp: ENST00000607266.1:c.384G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.367G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.453G>A
  hgvsp: ENST00000488034.1:c.453G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.403G>A
  hgvsp: ENSP00000418612.1:p.Ala135Thr
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.510G>A
  hgvsp: ENST00000374500.5:c.510G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.384G>A
  hgvsp: ENST00000440279.3:c.384G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.372+12G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.384G>A
  hgvsp: ENST00000374496.3:c.384G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*136G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1202G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*414G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.775G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.759G>A
  variant of: http://identifiers.org/hgnc/21101
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5322
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7233
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala135Thr
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

6-33384516-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384516
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384516
    reference: chr 6
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.757T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.382T>C
  hgvsp: ENST00000607266.1:c.382T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.401T>C
  hgvsp: ENSP00000418612.1:p.Ile134Thr
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.382T>C
  hgvsp: ENST00000374496.3:c.382T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.773T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.508T>C
  hgvsp: ENST00000374500.5:c.508T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.451T>C
  hgvsp: ENST00000488034.1:c.451T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1200T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*134T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.382T>C
  hgvsp: ENST00000440279.3:c.382T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.372+10T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*412T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.365T>C
  variant of: http://identifiers.org/hgnc/21101
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11352
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8748
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1300
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7235
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ile134Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

6-33384521-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384521
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384521
    reference: chr 6
allele count: 6
allele frequency: 4.943886883868097e-5
allele num: 121362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.377T>C
  hgvsp: ENSP00000403268.2:p.Ile126Thr
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*129T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.377T>C
  hgvsp: ENSP00000363620.3:p.Ile126Thr
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.752T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.372+5T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.377T>C
  hgvsp: ENSP00000475963.1:p.Ile126Thr
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.396T>C
  hgvsp: ENST00000488478.1:c.396T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.446T>C
  hgvsp: ENSP00000417544.1:p.Ile149Thr
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*407T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.503T>C
  hgvsp: ENSP00000363624.5:p.Ile168Thr
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.360T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.768T>C
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1195T>C
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7702
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile168Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: A
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

6-33384528-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384528
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384528
    reference: chr 6
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363624
  ensembl transcript: ENST00000374500
  gene symbol: CUTA
  hgvsc: ENST00000374500.5:c.496G>A
  hgvsp: ENSP00000363624.5:p.Glu166Lys
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.389G>A
  hgvsp: ENSP00000418612.1:p.Arg130Gln
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.370G>A
  hgvsp: ENSP00000475963.1:p.Glu124Lys
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000487637
  gene symbol: CUTA
  hgvsc: ENST00000487637.1:n.1188G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363608
  ensembl transcript: ENST00000374484
  gene symbol: CUTA
  hgvsc: ENST00000374484.4:c.*122G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.370G>A
  hgvsp: ENSP00000363620.3:p.Glu124Lys
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*400G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418659
  ensembl transcript: ENST00000494751
  gene symbol: CUTA
  hgvsc: ENST00000494751.1:c.370G>A
  hgvsp: ENSP00000418659.1:p.Glu124Lys
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000465956
  gene symbol: CUTA
  hgvsc: ENST00000465956.1:n.761G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000403268
  ensembl transcript: ENST00000440279
  gene symbol: CUTA
  hgvsc: ENST00000440279.3:c.370G>A
  hgvsp: ENSP00000403268.2:p.Glu124Lys
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.353G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000462802
  gene symbol: CUTA
  hgvsc: ENST00000462802.1:n.745G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417544
  ensembl transcript: ENST00000488034
  gene symbol: CUTA
  hgvsc: ENST00000488034.1:c.439G>A
  hgvsp: ENSP00000417544.1:p.Glu147Lys
  variant of: http://identifiers.org/hgnc/21101
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8746
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11328
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10700
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu166Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

6-33384532-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 33384532
    reference: chr 6
  end: Position
    type: ExactPosition
    position: 33384532
    reference: chr 6
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000363620
  ensembl transcript: ENST00000374496
  gene symbol: CUTA
  hgvsc: ENST00000374496.3:c.366G>A
  hgvsp: ENST00000374496.3:c.366G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000475963
  ensembl transcript: ENST00000607266
  gene symbol: CUTA
  hgvsc: ENST00000607266.1:c.366G>A
  hgvsp: ENST00000607266.1:c.366G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000417823
  ensembl transcript: ENST00000482684
  gene symbol: CUTA
  hgvsc: ENST00000482684.1:c.*396G>A
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000112514
  ensembl protein: ENSP00000418612
  ensembl transcript: ENST00000488478
  gene symbol: CUTA
  hgvsc: ENST00000488478.1:c.385G>A
  hgvsp: ENSP00000418612.1:p.Gly129Ser
  variant of: http://identifiers.org/hgnc/21101
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000112514
  ensembl transcript: ENST00000479249
  gene symbol: CUTA
  hgvsc: ENST00000479249.1:n.349G>A
  variant of: http://identifiers.org/hgnc/21101
canonical: false
consequence: missense
filter: PASS
hgvs: p.Gly129Ser
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 15516
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 198
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3054
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6808
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4755
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.528350909368791e-5
allele num: 65430
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14284
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.945e1

VQSLOD
type: SiteQuality
SIO_000300: 3.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

DP
type: SiteQuality
SIO_000300: 2.126453e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.1e-1

QD
type: SiteQuality
SIO_000300: 1.297e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

GenotypeQuality
all individuals: 3369
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6808
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4755
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3157
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15516
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 186
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3054
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.000840100812098e-5
allele num: 14284
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65430
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10214
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

QD
type: SiteQuality
SIO_000300: 1.297e1

DP
type: SiteQuality
SIO_000300: 2.126453e6

MQRankSum
type: SiteQuality
SIO_000300: -1.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

VQSLOD
type: SiteQuality
SIO_000300: 3.1e0

GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2139
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4249
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3368
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 7.5e0
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13570
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.811616954474098e-5
allele num: 10192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65132
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.29e-1

QD
type: SiteQuality
SIO_000300: 1.075e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 2.111888e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.757e0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6735
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4747
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3367
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10132
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12768
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8462
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.544974198930878e-5
allele num: 64726
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.368e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.507e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.756e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 4.57e0

DP
type: SiteQuality
SIO_000300: 2.097704e6

GenotypeQuality
all individuals: 154
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2999
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4735
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2138
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6582
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8348
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9900
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9938
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 794
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.583531274742676e-5
allele num: 63150
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.9e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.57e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 1.279e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.13e0

MQRankSum
type: SiteQuality
SIO_000300: 6.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

DP
type: SiteQuality
SIO_000300: 2.055735e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.365e0

GenotypeQuality
all individuals: 2874
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2992
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6581
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2996
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9856
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63096
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11398
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.011326860841424e-4
allele num: 9888
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.129999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.13e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e-1

DP
type: SiteQuality
SIO_000300: 2.054407e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.202e1

GenotypeQuality
all individuals: 3365
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15497
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 50
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.187454180346157e-5
allele num: 62746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9254
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9826
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8294
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.33e1

FS
type: SiteQuality
SIO_000300: 4.445e0

MQRankSum
type: SiteQuality
SIO_000300: -5.058e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.37e0

DP
type: SiteQuality
SIO_000300: 2.040227e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

QD
type: SiteQuality
SIO_000300: 4.1e0

GenotypeQuality
all individuals: 4691
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2963
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15476
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 97
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9038
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11366
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9806
num of homozygotes: 0

East Asian
type: Population
allele count: 10
allele frequency: 1.209774981853375e-3
allele num: 8266
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.624e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.1e-3

MQ
type: SiteQuality
SIO_000300: 5.952e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.1e0

MQRankSum
type: SiteQuality
SIO_000300: 6.67e-1

DP
type: SiteQuality
SIO_000300: 2.022528e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.36e-1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15469
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4204
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4685
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9804
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.198362438431523e-5
allele num: 62532
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9036
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6432
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.76e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -6.94e-1

FS
type: SiteQuality
SIO_000300: 1.0785e1

QD
type: SiteQuality
SIO_000300: 1.637e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

DP
type: SiteQuality
SIO_000300: 2.02123e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 8.79e-1

GenotypeQuality
all individuals: 1865
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 6326
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variant carriers: 0

GenotypeQuality
all individuals: 4186
bin: 8.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9028
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6430
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.600102406554019e-5
allele num: 62496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11362
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.199999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.143e0

QD
type: SiteQuality
SIO_000300: 2.42e1

DP
type: SiteQuality
SIO_000300: 2.0183e6

MQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.355e0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15447
bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9776
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11354
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9014
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8262
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.013018e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 2.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.98e-1

QD
type: SiteQuality
SIO_000300: 1.624e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

MQRankSum
type: SiteQuality
SIO_000300: -1.98e-1

GenotypeQuality
all individuals: 226
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4147
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11354
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4598
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.604775812818949e-5
allele num: 62314
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9766
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8248
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.78e0

VQSLOD
type: SiteQuality
SIO_000300: -1.001e0

QD
type: SiteQuality
SIO_000300: 1.08e1

DP
type: SiteQuality
SIO_000300: 1.988116e6

FS
type: SiteQuality
SIO_000300: 2.077e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.37e-1

MQ
type: SiteQuality
SIO_000300: 5.89e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.44e-1

GenotypeQuality
all individuals: 3532
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 849
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4135
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4564
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62258
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.113089937666963e-4
allele num: 8984
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11348
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.062e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.981408e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.81e0

QD
type: SiteQuality
SIO_000300: 1.205e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.9e-2

MQRankSum
type: SiteQuality
SIO_000300: -6.74e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 271
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variant carriers: 0

GenotypeQuality
all individuals: 15424
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.812125484666901e-5
allele num: 11348
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8984
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6392
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.933e1

MQRankSum
type: SiteQuality
SIO_000300: -6.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.062e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.205e1

DP
type: SiteQuality
SIO_000300: 1.981408e6

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15416
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.2139872726104e-5
allele num: 62228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11348
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8246
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8988
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

FS
type: SiteQuality
SIO_000300: 2.464e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

QD
type: SiteQuality
SIO_000300: 1.093e1

MQRankSum
type: SiteQuality
SIO_000300: -9.429999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

DP
type: SiteQuality
SIO_000300: 1.97717e6

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9738
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6376
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8250
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8978
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62212
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.76242509693338e-4
allele num: 11348
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.91e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.037e0

DP
type: SiteQuality
SIO_000300: 1.966141e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.49e-1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.2e-1

FS
type: SiteQuality
SIO_000300: 6.223e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8248
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6370
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.218124477054773e-5
allele num: 62148
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8978
num of homozygotes: 0

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

FS
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

DP
type: SiteQuality
SIO_000300: 1.956459e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.507e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6376
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.816787162757891e-5
allele num: 11342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62128
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9724
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8250
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.955727e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.566e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.17e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -6.51e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.14e-1

QD
type: SiteQuality
SIO_000300: 1.403e1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8240
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6356
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.821453775582216e-5
allele num: 11336
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9728
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62068
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8974
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.599999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.62e-1

FS
type: SiteQuality
SIO_000300: 3.067e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e0

MQRankSum
type: SiteQuality
SIO_000300: 3.06e0

VQSLOD
type: SiteQuality
SIO_000300: -2.896e0

QD
type: SiteQuality
SIO_000300: 1.345e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.318e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

DP
type: SiteQuality
SIO_000300: 1.94803e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6356
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9728
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
allele num: 8240
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.114330287497214e-4
allele num: 8974
num of homozygotes: 0

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

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

DP
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 3.067e0

InbreedingCoeff
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SIO_000300: 9.599999999999999e-3

ClippingRankSum
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SIO_000300: 1.56e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.62e-1

QD
type: SiteQuality
SIO_000300: 1.345e1

VQSLOD
type: SiteQuality
SIO_000300: -2.896e0

MQRankSum
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SIO_000300: 3.06e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8234
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.029866117404737e-4
allele num: 9710
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62026
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8964
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.832361773538245e-5
allele num: 11322
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.12e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

VQSLOD
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InbreedingCoeff
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SIO_000300: -1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.16e-1

ReadPosRankSum
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SIO_000300: 1.35e0

DP
type: SiteQuality
SIO_000300: 1.942192e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.08e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

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

Latino
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allele frequency: 8.683570684265369e-5
allele num: 11516
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65790
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.9e-1

ReadPosRankSum
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MQRankSum
type: SiteQuality
SIO_000300: -1.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -2.74e-1

FS
type: SiteQuality
SIO_000300: 2.036e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.086e1

DP
type: SiteQuality
SIO_000300: 2.243869e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.682062858135092e-5
allele num: 11518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65804
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.359e0

FS
type: SiteQuality
SIO_000300: 2.008e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.47e-1

DP
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SIO_000300: 2.245227e6

ReadPosRankSum
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SIO_000300: -8.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

QD
type: SiteQuality
SIO_000300: 1.229e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.517865274278255e-5
allele num: 65882
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

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

Other
type: Population
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allele frequency: 0.0e0
allele num: 882
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: 6614
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

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

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

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

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.517128379403465e-5
allele num: 65914
num of homozygotes: 0

Other
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ClippingRankSum
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MQRankSum
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DP
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MQ
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VQSLOD
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BaseQRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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QD
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GenotypeDepth
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variant carriers: 3

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
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: 1.127689104788341e-3
allele num: 11528
num of homozygotes: 0

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

European (Non-Finnish)
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num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
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allele frequency: 1.514692517418964e-5
allele num: 66020
num of homozygotes: 0

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

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

FS
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QD
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ClippingRankSum
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ReadPosRankSum
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DP
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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BaseQRankSum
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SIO_000300: -2.707e0

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

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

European (Non-Finnish)
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allele frequency: 1.515151515151515e-5
allele num: 66000
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

Other
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African
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allele count: 1
allele frequency: 9.780907668231612e-5
allele num: 10224
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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FS
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MQRankSum
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QD
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ReadPosRankSum
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MQ
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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DP
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ClippingRankSum
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SIO_000300: -8.070000000000001e-1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10224
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 66000
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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East Asian
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Latino
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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

InbreedingCoeff
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MQ
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QD
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BaseQRankSum
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FS
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VQSLOD
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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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

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

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

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
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InbreedingCoeff
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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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VQSLOD
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DP
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BaseQRankSum
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QD
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GenotypeDepth
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variant carriers: 1

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66126
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

Other
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num of homozygotes: 0

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

European (Finnish)
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num of homozygotes: 0

African
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allele frequency: 5.836575875486381e-4
allele num: 10280
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East Asian
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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QD
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ClippingRankSum
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MQ
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

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: 1
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allele num: 66150
num of homozygotes: 0

Other
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Latino
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South Asian
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European (Finnish)
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QD
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 num: 15986
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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Other
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European (Finnish)
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East Asian
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European (Non-Finnish)
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allele num: 66150
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FS
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DP
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MQ
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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QD
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MQRankSum
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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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num of homozygotes: 0

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

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

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

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

European (Finnish)
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allele frequency: 0.0e0
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Latino
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South Asian
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.504347564461293e-5
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ClippingRankSum
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DP
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BaseQRankSum
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FS
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QD
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MQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 10336
num of homozygotes: 0

European (Finnish)
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allele count: 0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.503714174009804e-5
allele num: 66502
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Other
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South Asian
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East Asian
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InbreedingCoeff
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MQRankSum
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DP
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MQ
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BaseQRankSum
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QD
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ReadPosRankSum
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VQSLOD
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FS
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

South Asian
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allele frequency: 2.43516376476318e-4
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European (Non-Finnish)
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allele num: 66502
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African
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Latino
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European (Finnish)
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Other
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DP
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FS
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QD
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MQRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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East Asian
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num of homozygotes: 0

European (Non-Finnish)
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Other
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South Asian
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European (Finnish)
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DP
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FS
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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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ReadPosRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

South Asian
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European (Finnish)
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allele num: 6614
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Latino
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Other
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East Asian
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European (Non-Finnish)
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VQSLOD
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ClippingRankSum
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FS
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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DP
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MQ
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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African
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East Asian
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Other
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European (Finnish)
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South Asian
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
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MQ
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QD
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InbreedingCoeff
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66634
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Other
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South Asian
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African
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Latino
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European (Finnish)
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East Asian
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MQ
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FS
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ReadPosRankSum
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DP
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InbreedingCoeff
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BaseQRankSum
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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African
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East Asian
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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DP
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FS
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InbreedingCoeff
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MQ
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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East Asian
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European (Non-Finnish)
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South Asian
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DP
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ClippingRankSum
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MQRankSum
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FS
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QD
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MQ
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BaseQRankSum
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African
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South Asian
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East Asian
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FS
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VQSLOD
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MQ
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DP
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ReadPosRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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European (Finnish)
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ReadPosRankSum
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DP
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VQSLOD
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MQRankSum
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FS
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MQ
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GenotypeDepth
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South Asian
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African
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VQSLOD
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DP
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FS
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QD
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InbreedingCoeff
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MQRankSum
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South Asian
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African
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VQSLOD
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MQRankSum
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DP
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BaseQRankSum
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.029935765361775e-4
allele num: 16502
num of homozygotes: 0

African
type: Population
allele count: 40
allele frequency: 3.857280617164899e-3
allele num: 10370
num of homozygotes: 0

Other
type: Population
allele count: 7
allele frequency: 7.72626931567329e-3
allele num: 906
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 255
allele frequency: 3.855458119141215e-2
allele num: 6614
num of homozygotes: 2

Latino
type: Population
allele count: 17
allele frequency: 1.470333852274693e-3
allele num: 11562
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 2141
allele frequency: 3.210954137796575e-2
allele num: 66678
num of homozygotes: 54

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 2.569e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.06e-1

QD
type: SiteQuality
SIO_000300: 1.245e1

VQSLOD
type: SiteQuality
SIO_000300: 3.06e0

DP
type: SiteQuality
SIO_000300: 2.383708e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.23e-2

GenotypeDepth
all individuals: 3405
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 356
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5322
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variant carriers: 3

GenotypeDepth
all individuals: 133
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variant carriers: 1

GenotypeDepth
all individuals: 532
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variant carriers: 2

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 3664
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variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 20436
bin: 9.75e1
variant carriers: 18

Latino
type: Population
allele count: 14
allele frequency: 1.210863172461512e-3
allele num: 11562
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21197430614471e-4
allele num: 16502
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
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: 5.27e-1

DP
type: SiteQuality
SIO_000300: 2.297853e6

VQSLOD
type: SiteQuality
SIO_000300: 2.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.084e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.01e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.24e-1

QD
type: SiteQuality
SIO_000300: 1.348e1

GenotypeDepth
all individuals: 64
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 137
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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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GenotypeQuality
all individuals: 3669
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 4772
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 6699
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 14789
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GenotypeQuality
all individuals: 20422
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variant carriers: 1

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 72
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3426
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variant carriers: 0

GenotypeQuality
all individuals: 2555
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variant carriers: 0

GenotypeQuality
all individuals: 4174
bin: 8.25e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
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: 908
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.2e0

MQ
type: SiteQuality
SIO_000300: 5.888e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.435e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.836e0

MQRankSum
type: SiteQuality
SIO_000300: -8.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.579e0

DP
type: SiteQuality
SIO_000300: 2.297645e6

QD
type: SiteQuality
SIO_000300: 1.563e1

GenotypeDepth
all individuals: 509
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 235
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 355
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1300
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variant carriers: 0

GenotypeDepth
all individuals: 802
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variant carriers: 0

GenotypeQuality
all individuals: 4173
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 2556
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 3427
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20422
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variant carriers: 1

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 4776
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 14791
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GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 6700
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variant carriers: 0

GenotypeQuality
all individuals: 22
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GenotypeQuality
all individuals: 3678
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variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499385252046661e-5
allele num: 66694
num of homozygotes: 0

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

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

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

European (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: 8654
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 7.94e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.04e-1

DP
type: SiteQuality
SIO_000300: 2.298094e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.602e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.04e-1

QD
type: SiteQuality
SIO_000300: 1.382e1

FS
type: SiteQuality
SIO_000300: 2.619e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.419999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeDepth
all individuals: 802
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8745
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 530
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variant carriers: 0

GenotypeDepth
all individuals: 11300
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variant carriers: 0

GenotypeDepth
all individuals: 356
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variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6691
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2557
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 56
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variant carriers: 0

GenotypeQuality
all individuals: 14795
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 3427
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 20423
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4780
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 3680
bin: 7.25e1
variant carriers: 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: 8654
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

QD
type: SiteQuality
SIO_000300: 1.444e1

DP
type: SiteQuality
SIO_000300: 2.298484e6

MQRankSum
type: SiteQuality
SIO_000300: -6.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

MQ
type: SiteQuality
SIO_000300: 5.915e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 1300
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5320
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 138
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 235
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 802
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variant carriers: 0

GenotypeQuality
all individuals: 14795
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3680
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

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

GenotypeQuality
all individuals: 22
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 20423
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 18
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GenotypeQuality
all individuals: 4780
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3427
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 1
allele frequency: 9.624639076034648e-5
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499250374812594e-5
allele num: 66700
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.298484e6

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

MQ
type: SiteQuality
SIO_000300: 5.915e1

FS
type: SiteQuality
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 3.94e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.86e-1

QD
type: SiteQuality
SIO_000300: 1.444e1

GenotypeDepth
all individuals: 235
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 137
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variant carriers: 0

GenotypeDepth
all individuals: 1300
bin: 6.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
all individuals: 4778
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 22
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GenotypeQuality
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GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 14809
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
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: 6614
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499160470136723e-5
allele num: 66704
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.062e0

DP
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VQSLOD
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
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InbreedingCoeff
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SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 1.41e0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
all individuals: 509
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variant carriers: 0

GenotypeDepth
all individuals: 137
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variant carriers: 0

GenotypeDepth
all individuals: 2143
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GenotypeDepth
all individuals: 235
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

South Asian
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allele num: 16506
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11568
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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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FS
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ClippingRankSum
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MQ
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16504
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

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

VQSLOD
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MQ
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DP
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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QD
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FS
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SIO_000300: 1.728e0

MQRankSum
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SIO_000300: 1.09e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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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

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

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

East Asian
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allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

InbreedingCoeff
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VQSLOD
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FS
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DP
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 5.977e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeQuality
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bin: 9.75e1
variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
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allele count: 5
allele frequency: 7.495128166691651e-5
allele num: 66710
num of homozygotes: 0

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

South Asian
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allele count: 0
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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East Asian
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allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

South Asian
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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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: 6

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.496942079386017e-5
allele num: 66712
num of homozygotes: 0

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

East Asian
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allele frequency: 2.31107002542177e-4
allele num: 8654
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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.859e0

DP
type: SiteQuality
SIO_000300: 2.298462e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.189e0

MQRankSum
type: SiteQuality
SIO_000300: -4.94e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.93e0

QD
type: SiteQuality
SIO_000300: 1.306e1

GenotypeDepth
all individuals: 5318
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 531
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 133
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1301
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 137
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 800
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6670
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14762
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3669
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2544
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4172
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20404
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 28
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3419
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4766
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
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: 906
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.297898e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.319e0

QD
type: SiteQuality
SIO_000300: 1.034e1

FS
type: SiteQuality
SIO_000300: 5.4e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.649999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

MQRankSum
type: SiteQuality
SIO_000300: 1.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.59e-1