3-50099027-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099027
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099027
    reference: chr 3
allele count: 1
allele frequency: 1.14710470771772e-5
allele num: 87176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.2090A>T
  hgvsp: ENSP00000406548.1:p.Gln697Leu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.465+47A>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.873+47A>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2439+47A>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*743+47A>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.873+47A>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2043+47A>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1378+47A>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*290+47A>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.183+47A>T
  variant of: http://identifiers.org/hgnc/9903
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8530
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4528
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15071
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10943
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3356
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln697Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

3-50099028-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099028
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099028
    reference: chr 3
allele count: 3
allele frequency: 3.492758347692451e-5
allele num: 85892
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.2091A>G
  hgvsp: ENST00000454079.1:c.2091A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2439+48A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.873+48A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.183+48A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*743+48A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*290+48A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2043+48A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1378+48A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.873+48A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.465+48A>G
  variant of: http://identifiers.org/hgnc/9903
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15535
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11882
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8397
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 705
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3624
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3384
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gln697Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS

3-50099038-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099038
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099038
    reference: chr 3
allele count: 1
allele frequency: 1.240294694019299e-5
allele num: 80626
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*743+58T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*7T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*290+58T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2439+58T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.183+58T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1378+58T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2043+58T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.465+58T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.873+58T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.873+58T>C
  variant of: http://identifiers.org/hgnc/9903
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19037
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7876
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13892
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4107
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1520
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/3-50099049-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099049
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099049
    reference: chr 3
allele count: 1
allele frequency: 1.391865935473095e-5
allele num: 71846
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.465+69C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*290+69C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1378+69C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*743+69C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2439+69C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.873+69C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*18C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2043+69C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.873+69C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.183+69C>A
  variant of: http://identifiers.org/hgnc/9903
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15915
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4861
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21470
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5934
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4004
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4579
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 212
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/3-50099052-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099052
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099052
    reference: chr 3
allele count: 1
allele frequency: 1.44121292479751e-5
allele num: 69386
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.873+72A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2043+72A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.183+72A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.465+72A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2439+72A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*21A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*290+72A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*743+72A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1378+72A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.873+72A>C
  variant of: http://identifiers.org/hgnc/9903
canonical: false
consequence: 3' UTR
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 6749
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5183
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16604
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21341
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4842
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7258
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS

3-50099069-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099069
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099069
    reference: chr 3
allele count: 2
allele frequency: 3.484563384207959e-5
allele num: 57396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*38G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2043+89G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.873+89G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*743+89G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*290+89G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2439+89G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1378+89G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.873+89G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.465+89G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.183+89G>A
  variant of: http://identifiers.org/hgnc/9903
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6667
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20601
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8983
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2148
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17139
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9418
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/3-50099078-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099078
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099078
    reference: chr 3
allele count: 1
allele frequency: 1.908396946564886e-5
allele num: 52400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.873+98C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*47C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2043+98C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.465+98C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1378+98C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*743+98C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.873+98C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2439+98C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*290+98C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.183+98C>A
  variant of: http://identifiers.org/hgnc/9903
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9150
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15435
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2608
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2461
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3179
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

3-50099390-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099390
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099390
    reference: chr 3
allele count: 5
allele frequency: 4.145799475970946e-5
allele num: 120604
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*744-5C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1379-5C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.874-5C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*291-5C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.874-5C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.184-5C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2440-5C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2044-5C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*359C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.466-5C>T
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16599
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 772
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16931
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 2.75e1
  variant carriers: 0
hgvs: c.2440-5C>T
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

3-50099391-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099391
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099391
    reference: chr 3
allele count: 7
allele frequency: 5.800848581278176e-5
allele num: 120672
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.466-4G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1379-4G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*360G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2044-4G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.874-4G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*744-4G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.874-4G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.184-4G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*291-4G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2440-4G>A
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9921
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16696
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
hgvs: c.2440-4G>A
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

3-50099403-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099403
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099403
    reference: chr 3
allele count: 1
allele frequency: 8.269109913008963e-6
allele num: 120932
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.882C>T
  hgvsp: ENST00000442092.1:c.882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1387C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*372C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.474C>T
  hgvsp: ENST00000539992.1:c.474C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*752C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.192C>T
  hgvsp: ENST00000438912.1:c.192C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.882C>T
  hgvsp: ENST00000422955.1:c.882C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*299C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2052C>T
  hgvsp: ENST00000443081.1:c.2052C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2448C>T
  hgvsp: ENST00000266022.4:c.2448C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5441
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17052
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7302
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val816Val
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ

3-50099405-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099405
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099405
    reference: chr 3
allele count: 1
allele frequency: 8.267195767195768e-6
allele num: 120960
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*754A>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2450A>T
  hgvsp: ENSP00000266022.4:p.Tyr817Phe
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2054A>T
  hgvsp: ENSP00000396466.1:p.Tyr685Phe
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.476A>T
  hgvsp: ENSP00000443165.1:p.Tyr159Phe
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.884A>T
  hgvsp: ENSP00000392939.1:p.Tyr295Phe
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*374A>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*301A>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.884A>T
  hgvsp: ENSP00000393530.1:p.Tyr295Phe
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.194A>T
  hgvsp: ENSP00000403865.1:p.Tyr65Phe
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1389A>T
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17084
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5439
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17040
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Tyr817Phe
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: DP
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

3-50099412-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099412
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099412
    reference: chr 3
allele count: 1
allele frequency: 8.26296045347127e-6
allele num: 121022
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2061C>T
  hgvsp: ENST00000443081.1:c.2061C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*761C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*381C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.201C>T
  hgvsp: ENST00000438912.1:c.201C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.483C>T
  hgvsp: ENST00000539992.1:c.483C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2457C>T
  hgvsp: ENST00000266022.4:c.2457C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*308C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.891C>T
  hgvsp: ENST00000442092.1:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.891C>T
  hgvsp: ENST00000422955.1:c.891C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1396C>T
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17261
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5453
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10025
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro819Pro
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-50099414-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099414
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099414
    reference: chr 3
allele count: 7
allele frequency: 5.781397115908753e-5
allele num: 121078
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2459A>G
  hgvsp: ENSP00000266022.4:p.Gln820Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2063A>G
  hgvsp: ENSP00000396466.1:p.Gln688Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*383A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*310A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.485A>G
  hgvsp: ENSP00000443165.1:p.Gln162Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.893A>G
  hgvsp: ENSP00000393530.1:p.Gln298Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.893A>G
  hgvsp: ENSP00000392939.1:p.Gln298Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1398A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*763A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.203A>G
  hgvsp: ENSP00000403865.1:p.Gln68Arg
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16897
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gln820Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff

3-50099420-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099420
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099420
    reference: chr 3
allele count: 1
allele frequency: 8.25695648583932e-6
allele num: 121110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.899C>T
  hgvsp: ENSP00000393530.1:p.Pro300Leu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2465C>T
  hgvsp: ENSP00000266022.4:p.Pro822Leu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.899C>T
  hgvsp: ENSP00000392939.1:p.Pro300Leu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*316C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1404C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2069C>T
  hgvsp: ENSP00000396466.1:p.Pro690Leu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.491C>T
  hgvsp: ENSP00000443165.1:p.Pro164Leu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.209C>T
  hgvsp: ENSP00000403865.1:p.Pro70Leu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*389C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*769C>T
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1146
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro822Leu
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/3-50099428-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099428
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099428
    reference: chr 3
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.907C>A
  hgvsp: ENSP00000392939.1:p.Pro303Thr
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2077C>A
  hgvsp: ENSP00000396466.1:p.Pro693Thr
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*324C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2473C>A
  hgvsp: ENSP00000266022.4:p.Pro825Thr
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*397C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1412C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*777C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.499C>A
  hgvsp: ENSP00000443165.1:p.Pro167Thr
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.907C>A
  hgvsp: ENSP00000393530.1:p.Pro303Thr
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.217C>A
  hgvsp: ENSP00000403865.1:p.Pro73Thr
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro825Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD

3-50099429-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099429
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099429
    reference: chr 3
allele count: 1
allele frequency: 8.253140319891718e-6
allele num: 121166
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*398C>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*778C>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1413C>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.218C>G
  hgvsp: ENSP00000403865.1:p.Pro73Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.908C>G
  hgvsp: ENSP00000392939.1:p.Pro303Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.908C>G
  hgvsp: ENSP00000393530.1:p.Pro303Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*325C>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2474C>G
  hgvsp: ENSP00000266022.4:p.Pro825Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.500C>G
  hgvsp: ENSP00000443165.1:p.Pro167Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2078C>G
  hgvsp: ENSP00000396466.1:p.Pro693Arg
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16632
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17556
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5458
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro825Arg
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

3-50099437-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099437
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099437
    reference: chr 3
allele count: 1
allele frequency: 8.252867871585376e-6
allele num: 121170
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*333G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2482G>A
  hgvsp: ENSP00000266022.4:p.Glu828Lys
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.508G>A
  hgvsp: ENSP00000443165.1:p.Glu170Lys
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.916G>A
  hgvsp: ENSP00000392939.1:p.Glu306Lys
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*786G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.226G>A
  hgvsp: ENSP00000403865.1:p.Glu76Lys
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.916G>A
  hgvsp: ENSP00000393530.1:p.Glu306Lys
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1421G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2086G>A
  hgvsp: ENSP00000396466.1:p.Glu696Lys
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*406G>A
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17670
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5450
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4175
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu828Lys
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

3-50099449-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099449
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099450
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 120758
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*806dupA
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.936dupA
  hgvsp: ENSP00000392939.1:p.Pro313ThrfsTer9
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1441dupA
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2106dupA
  hgvsp: ENSP00000396466.1:p.Pro703ThrfsTer9
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.936dupA
  hgvsp: ENSP00000393530.1:p.Pro313ThrfsTer9
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.528dupA
  hgvsp: ENSP00000443165.1:p.Pro177ThrfsTer9
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2502dupA
  hgvsp: ENSP00000266022.4:p.Pro835ThrfsTer9
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*353dupA
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.246dupA
  hgvsp: ENSP00000403865.1:p.Pro83ThrfsTer9
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*426dupA
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1147
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10306
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1772
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17693
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3171
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro835ThrfsTer9
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

3-50099450-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099450
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099450
    reference: chr 3
allele count: 1
allele frequency: 8.271024945411235e-6
allele num: 120904
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.521A>G
  hgvsp: ENSP00000443165.1:p.Glu174Gly
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2495A>G
  hgvsp: ENSP00000266022.4:p.Glu832Gly
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.239A>G
  hgvsp: ENSP00000403865.1:p.Glu80Gly
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*346A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.929A>G
  hgvsp: ENSP00000392939.1:p.Glu310Gly
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1434A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*799A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2099A>G
  hgvsp: ENSP00000396466.1:p.Glu700Gly
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*419A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.929A>G
  hgvsp: ENSP00000393530.1:p.Glu310Gly
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10258
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15764
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu832Gly
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

3-50099451-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099451
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099451
    reference: chr 3
allele count: 1
allele frequency: 8.257774694875225e-6
allele num: 121098
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.240A>G
  hgvsp: ENST00000438912.1:c.240A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*347A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.522A>G
  hgvsp: ENST00000539992.1:c.522A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1435A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.930A>G
  hgvsp: ENST00000422955.1:c.930A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.930A>G
  hgvsp: ENST00000442092.1:c.930A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2100A>G
  hgvsp: ENST00000443081.1:c.2100A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*800A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*420A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2496A>G
  hgvsp: ENST00000266022.4:c.2496A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10213
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu832Glu
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

3-50099452-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099452
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099452
    reference: chr 3
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1436A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2101A>G
  hgvsp: ENSP00000396466.1:p.Lys701Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*801A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2497A>G
  hgvsp: ENSP00000266022.4:p.Lys833Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*421A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.523A>G
  hgvsp: ENSP00000443165.1:p.Lys175Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.931A>G
  hgvsp: ENSP00000393530.1:p.Lys311Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.241A>G
  hgvsp: ENSP00000403865.1:p.Lys81Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.931A>G
  hgvsp: ENSP00000392939.1:p.Lys311Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*348A>G
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3048
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10126
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Lys833Glu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP

3-50099457-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099457
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099457
    reference: chr 3
allele count: 1
allele frequency: 8.25218682950982e-6
allele num: 121180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1441A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2106A>G
  hgvsp: ENST00000443081.1:c.2106A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*426A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.936A>G
  hgvsp: ENST00000422955.1:c.936A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.936A>G
  hgvsp: ENST00000442092.1:c.936A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.246A>G
  hgvsp: ENST00000438912.1:c.246A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*353A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.528A>G
  hgvsp: ENST00000539992.1:c.528A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2502A>G
  hgvsp: ENST00000266022.4:c.2502A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*806A>G
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15901
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5446
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys834Lys
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

3-50099463-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099463
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099463
    reference: chr 3
allele count: 1
allele frequency: 8.254366559910193e-6
allele num: 121148
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.942C>T
  hgvsp: ENST00000442092.1:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.534C>T
  hgvsp: ENST00000539992.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.942C>T
  hgvsp: ENST00000422955.1:c.942C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.252C>T
  hgvsp: ENST00000438912.1:c.252C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*359C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2112C>T
  hgvsp: ENST00000443081.1:c.2112C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2508C>T
  hgvsp: ENST00000266022.4:c.2508C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*432C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1447C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*812C>T
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 18168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15832
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10163
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5440
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr836Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP

3-50099465-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099465
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099465
    reference: chr 3
allele count: 1
allele frequency: 8.254094030639197e-6
allele num: 121152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.944G>T
  hgvsp: ENSP00000393530.1:p.Ser315Ile
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.944G>T
  hgvsp: ENSP00000392939.1:p.Ser315Ile
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2114G>T
  hgvsp: ENSP00000396466.1:p.Ser705Ile
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.536G>T
  hgvsp: ENSP00000443165.1:p.Ser179Ile
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2510G>T
  hgvsp: ENSP00000266022.4:p.Ser837Ile
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*361G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1449G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.254G>T
  hgvsp: ENSP00000403865.1:p.Ser85Ile
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*434G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*814G>T
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18251
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser837Ile
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/3-50099468-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099468
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099468
    reference: chr 3
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2117A>C
  hgvsp: ENSP00000396466.1:p.Gln706Pro
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.947A>C
  hgvsp: ENSP00000393530.1:p.Gln316Pro
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*437A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*817A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2513A>C
  hgvsp: ENSP00000266022.4:p.Gln838Pro
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1452A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.947A>C
  hgvsp: ENSP00000392939.1:p.Gln316Pro
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.539A>C
  hgvsp: ENSP00000443165.1:p.Gln180Pro
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*364A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.257A>C
  hgvsp: ENSP00000403865.1:p.Gln86Pro
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10110
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln838Pro
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/3-50099474-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099474
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099474
    reference: chr 3
allele count: 1
allele frequency: 8.25300409349003e-6
allele num: 121168
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*443A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2123A>C
  hgvsp: ENSP00000396466.1:p.Lys708Thr
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.263A>C
  hgvsp: ENSP00000403865.1:p.Lys88Thr
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2519A>C
  hgvsp: ENSP00000266022.4:p.Lys840Thr
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*370A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.545A>C
  hgvsp: ENSP00000443165.1:p.Lys182Thr
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.953A>C
  hgvsp: ENSP00000392939.1:p.Lys318Thr
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.953A>C
  hgvsp: ENSP00000393530.1:p.Lys318Thr
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*823A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1458A>C
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10100
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18270
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys840Thr
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

3-50099481-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099481
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099481
    reference: chr 3
allele count: 1
allele frequency: 8.254639107178234e-6
allele num: 121144
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2526T>A
  hgvsp: ENSP00000266022.4:p.Ser842Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2130T>A
  hgvsp: ENSP00000396466.1:p.Ser710Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1465T>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*830T>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.270T>A
  hgvsp: ENSP00000403865.1:p.Ser90Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*377T>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*450T>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.552T>A
  hgvsp: ENSP00000443165.1:p.Ser184Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.960T>A
  hgvsp: ENSP00000392939.1:p.Ser320Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.960T>A
  hgvsp: ENSP00000393530.1:p.Ser320Arg
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15886
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18256
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ser842Arg
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum

3-50099487-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099487
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099487
    reference: chr 3
allele count: 1
allele frequency: 8.255320554097116e-6
allele num: 121134
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.966G>T
  hgvsp: ENSP00000392939.1:p.Lys322Asn
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2532G>T
  hgvsp: ENSP00000266022.4:p.Lys844Asn
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*456G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.276G>T
  hgvsp: ENSP00000403865.1:p.Lys92Asn
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2136G>T
  hgvsp: ENSP00000396466.1:p.Lys712Asn
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.558G>T
  hgvsp: ENSP00000443165.1:p.Lys186Asn
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.966G>T
  hgvsp: ENSP00000393530.1:p.Lys322Asn
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*836G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1471G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*383G>T
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15899
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18250
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3177
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Lys844Asn
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP

3-50099500-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099500
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099500
    reference: chr 3
allele count: 120
allele frequency: 9.912440112340988e-4
allele num: 121060
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2545A>G
  hgvsp: ENSP00000266022.4:p.Lys849Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.979A>G
  hgvsp: ENSP00000392939.1:p.Lys327Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.979A>G
  hgvsp: ENSP00000393530.1:p.Lys327Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1484A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2149A>G
  hgvsp: ENSP00000396466.1:p.Lys717Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*396A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.289A>G
  hgvsp: ENSP00000403865.1:p.Lys97Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*469A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.571A>G
  hgvsp: ENSP00000443165.1:p.Lys191Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*849A>G
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15807
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5426
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 18223
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10071
  bin: 3.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 4.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 9.75e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys849Glu
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

3-50099508-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099508
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099508
    reference: chr 3
allele count: 1
allele frequency: 8.263233568560049e-6
allele num: 121018
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*477T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2553T>C
  hgvsp: ENST00000266022.4:c.2553T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.579T>C
  hgvsp: ENST00000539992.1:c.579T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*404T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2157T>C
  hgvsp: ENST00000443081.1:c.2157T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.987T>C
  hgvsp: ENST00000442092.1:c.987T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.297T>C
  hgvsp: ENST00000438912.1:c.297T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.987T>C
  hgvsp: ENST00000422955.1:c.987T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1492T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*857T>C
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5427
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2993
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp851Asp
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

3-50099512-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099512
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099512
    reference: chr 3
allele count: 26
allele frequency: 2.149364284179025e-4
allele num: 120966
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.583A>G
  hgvsp: ENSP00000443165.1:p.Lys195Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*408A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.301A>G
  hgvsp: ENSP00000403865.1:p.Lys101Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*481A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.991A>G
  hgvsp: ENSP00000392939.1:p.Lys331Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.991A>G
  hgvsp: ENSP00000393530.1:p.Lys331Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*861A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2557A>G
  hgvsp: ENSP00000266022.4:p.Lys853Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2161A>G
  hgvsp: ENSP00000396466.1:p.Lys721Glu
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1496A>G
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 15695
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 18188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10046
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 10848
  bin: 9.75e1
  variant carriers: 26
hgvs: p.Lys853Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP

3-50099519-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099519
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099519
    reference: chr 3
allele count: 1
allele frequency: 8.271298593879239e-6
allele num: 120900
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2564A>G
  hgvsp: ENSP00000266022.4:p.Lys855Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*868A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*415A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.998A>G
  hgvsp: ENSP00000392939.1:p.Lys333Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.590A>G
  hgvsp: ENSP00000443165.1:p.Lys197Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*488A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2168A>G
  hgvsp: ENSP00000396466.1:p.Lys723Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.998A>G
  hgvsp: ENSP00000393530.1:p.Lys333Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.308A>G
  hgvsp: ENSP00000403865.1:p.Lys103Arg
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1503A>G
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18189
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1691
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4067
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys855Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum

3-50099537-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099537
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099537
    reference: chr 3
allele count: 3
allele frequency: 2.491652962575373e-5
allele num: 120402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2186C>T
  hgvsp: ENSP00000396466.1:p.Thr729Met
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1016C>T
  hgvsp: ENSP00000393530.1:p.Thr339Met
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.608C>T
  hgvsp: ENSP00000443165.1:p.Thr203Met
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1521C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*886C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*433C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.326C>T
  hgvsp: ENSP00000403865.1:p.Thr109Met
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1016C>T
  hgvsp: ENSP00000392939.1:p.Thr339Met
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*506C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2582C>T
  hgvsp: ENSP00000266022.4:p.Thr861Met
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3050
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17851
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14563
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10020
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Thr861Met
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

3-50099538-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099538
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099538
    reference: chr 3
allele count: 2
allele frequency: 1.66237220513673e-5
allele num: 120310
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1522G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.609G>A
  hgvsp: ENST00000539992.1:c.609G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*507G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1017G>A
  hgvsp: ENST00000422955.1:c.1017G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1017G>A
  hgvsp: ENST00000442092.1:c.1017G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2583G>A
  hgvsp: ENST00000266022.4:c.2583G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.327G>A
  hgvsp: ENST00000438912.1:c.327G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*434G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*887G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2187G>A
  hgvsp: ENST00000443081.1:c.2187G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14324
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5420
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9977
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17756
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr861Thr
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

3-50099541-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099541
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099541
    reference: chr 3
allele count: 6
allele frequency: 4.989687978178431e-5
allele num: 120248
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*890G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.612G>T
  hgvsp: ENSP00000443165.1:p.Arg204Ser
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*437G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1525G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2586G>T
  hgvsp: ENSP00000266022.4:p.Arg862Ser
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1020G>T
  hgvsp: ENSP00000392939.1:p.Arg340Ser
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.330G>T
  hgvsp: ENSP00000403865.1:p.Arg110Ser
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1020G>T
  hgvsp: ENSP00000393530.1:p.Arg340Ser
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*510G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2190G>T
  hgvsp: ENSP00000396466.1:p.Arg730Ser
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9950
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17698
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5404
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg862Ser
num of homozygotes: 0
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-50099544-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099544
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099544
    reference: chr 3
allele count: 1
allele frequency: 8.321682977165302e-6
allele num: 120168
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1020+3A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*437+3A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*890+3A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2586+3A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.612+3A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*510+3A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.330+3A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1525+3A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1020+3A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2190+3A>G
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9888
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2046
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2586+3A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

3-50099577-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50099577
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50099577
    reference: chr 3
allele count: 1
allele frequency: 8.407883231317684e-6
allele num: 118936
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2190+36A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*437+36A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.330+36A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1020+36A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*890+36A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*510+36A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1020+36A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2586+36A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1525+36A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.612+36A>G
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1687
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 896
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9047
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6689
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3026
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9565
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3798
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1122
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3240
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

3-50102414-TCA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102414
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102412
    reference: chr 3
allele count: 1
allele frequency: 8.290499088045101e-6
allele num: 120620
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*511-49_*511-48delCA
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1021-49_1021-48delCA
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.331-49_331-48delCA
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1526-49_1526-48delCA
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2587-49_2587-48delCA
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*438-49_*438-48delCA
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1021-49_1021-48delCA
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2191-49_2191-48delCA
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*891-49_*891-48delCA
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.613-49_613-48delCA
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2697
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6059
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6004
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2545
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3174
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: European (Finnish)
reference allele: TCA
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

3-50102417-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102417
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102417
    reference: chr 3
allele count: 1
allele frequency: 8.288849839196314e-6
allele num: 120644
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2587-47G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2191-47G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*438-47G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1526-47G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*511-47G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*891-47G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.613-47G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1021-47G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.331-47G>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1021-47G>T
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5700
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6059
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1726
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5520
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

3-50102424-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102424
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102424
    reference: chr 3
allele count: 1
allele frequency: 8.286239870071759e-6
allele num: 120682
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1021-40T>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2191-40T>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1526-40T>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.331-40T>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.613-40T>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2587-40T>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1021-40T>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*511-40T>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*438-40T>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*891-40T>A
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6058
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6004
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3182
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/3-50102426-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102426
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102426
    reference: chr 3
allele count: 3
allele frequency: 2.485830764641543e-5
allele num: 120684
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2587-38A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.613-38A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1526-38A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*438-38A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1021-38A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*511-38A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1021-38A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*891-38A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2191-38A>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.331-38A>C
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5700
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6004
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6057
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8238
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

3-50102427-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102427
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102427
    reference: chr 3
allele count: 1
allele frequency: 8.284866862189524e-6
allele num: 120702
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2587-37G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1021-37G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*438-37G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*511-37G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.331-37G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1021-37G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1526-37G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2191-37G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*891-37G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.613-37G>A
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5700
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5372
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

3-50102441-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102441
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102441
    reference: chr 3
allele count: 1
allele frequency: 8.269930532583527e-6
allele num: 120920
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*511-23A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*438-23A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.613-23A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1021-23A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.331-23A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2191-23A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1526-23A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*891-23A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2587-23A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1021-23A>G
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2498
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4228
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4982
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5701
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3272
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6053
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6006
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2552
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-50102446-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102446
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102446
    reference: chr 3
allele count: 8035
allele frequency: 6.638082019761408e-2
allele num: 121044
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1021-18T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1021-18T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1526-18T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*438-18T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2587-18T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*891-18T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*511-18T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.331-18T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2191-18T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.613-18T>C
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4981
  bin: 5.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 5643
  bin: 3.75e1
  variant carriers: 172
genotype depth: GenotypeDepth
  all individuals: 7603
  bin: 9.75e1
  variant carriers: 6326
genotype depth: GenotypeDepth
  all individuals: 4207
  bin: 5.75e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 5022
  bin: 2.75e1
  variant carriers: 232
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 3.25e1
  variant carriers: 276
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 9.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 8.75e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 2.25e1
  variant carriers: 162
genotype depth: GenotypeDepth
  all individuals: 3205
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 2396
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 7.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 6098
  bin: 4.25e1
  variant carriers: 111
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 4.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 8.25e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 2576
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 36975
  bin: 9.75e1
  variant carriers: 7636
num of homozygotes: 348
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

3-50102461-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102461
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102461
    reference: chr 3
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*438-3C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*891-3C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*511-3C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.613-3C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1526-3C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2587-3C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1021-3C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.331-3C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2191-3C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1021-3C>T
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4745
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6245
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2587-3C>T
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

3-50102477-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102477
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102477
    reference: chr 3
allele count: 1
allele frequency: 8.241848811525402e-6
allele num: 121332
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*451C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2204C>T
  hgvsp: ENSP00000396466.1:p.Ala735Val
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.626C>T
  hgvsp: ENSP00000443165.1:p.Ala209Val
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2600C>T
  hgvsp: ENSP00000266022.4:p.Ala867Val
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1034C>T
  hgvsp: ENSP00000392939.1:p.Ala345Val
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*524C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1034C>T
  hgvsp: ENSP00000393530.1:p.Ala345Val
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.344C>T
  hgvsp: ENSP00000403865.1:p.Ala115Val
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*904C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1539C>T
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6249
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4857
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5682
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala867Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

3-50102480-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102480
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102480
    reference: chr 3
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1037G>A
  hgvsp: ENSP00000392939.1:p.Ser346Asn
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*907G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1542G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1037G>A
  hgvsp: ENSP00000393530.1:p.Ser346Asn
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.347G>A
  hgvsp: ENSP00000403865.1:p.Ser116Asn
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*527G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2207G>A
  hgvsp: ENSP00000396466.1:p.Ser736Asn
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.629G>A
  hgvsp: ENSP00000443165.1:p.Ser210Asn
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2603G>A
  hgvsp: ENSP00000266022.4:p.Ser868Asn
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*454G>A
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5684
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1728
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser868Asn
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ

3-50102480-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102480
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102480
    reference: chr 3
allele count: 6
allele frequency: 4.945027774572667e-5
allele num: 121334
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*907G>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.629G>C
  hgvsp: ENSP00000443165.1:p.Ser210Thr
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1037G>C
  hgvsp: ENSP00000392939.1:p.Ser346Thr
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*454G>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1037G>C
  hgvsp: ENSP00000393530.1:p.Ser346Thr
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1542G>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2603G>C
  hgvsp: ENSP00000266022.4:p.Ser868Thr
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2207G>C
  hgvsp: ENSP00000396466.1:p.Ser736Thr
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000403865
  ensembl transcript: ENST00000438912
  gene symbol: RBM6
  hgvsc: ENST00000438912.1:c.347G>C
  hgvsp: ENSP00000403865.1:p.Ser116Thr
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*527G>C
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2731
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4855
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5684
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser868Thr
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

3-50102500-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102500
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102500
    reference: chr 3
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2623G>A
  hgvsp: ENSP00000266022.4:p.Glu875Lys
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*547G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1057G>A
  hgvsp: ENSP00000392939.1:p.Glu353Lys
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2227G>A
  hgvsp: ENSP00000396466.1:p.Glu743Lys
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1057G>A
  hgvsp: ENSP00000393530.1:p.Glu353Lys
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1562G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.649G>A
  hgvsp: ENSP00000443165.1:p.Glu217Lys
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*474G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*927G>A
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6806
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4744
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6236
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5683
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33449
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu875Lys
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum

3-50102505-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102505
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102505
    reference: chr 3
allele count: 243
allele frequency: 2.002340183589051e-3
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1567C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2628C>T
  hgvsp: ENST00000266022.4:c.2628C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*552C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.654C>T
  hgvsp: ENST00000539992.1:c.654C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2232C>T
  hgvsp: ENST00000443081.1:c.2232C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1062C>T
  hgvsp: ENST00000422955.1:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1062C>T
  hgvsp: ENST00000442092.1:c.1062C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*479C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*932C>T
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5687
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 9.75e1
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 6233
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3659
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4743
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6268
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6804
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6495
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2774
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1660
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asp876Asp
num of homozygotes: 1
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

3-50102530-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102530
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102530
    reference: chr 3
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2257A>G
  hgvsp: ENSP00000396466.1:p.Thr753Ala
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1087A>G
  hgvsp: ENSP00000393530.1:p.Thr363Ala
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*504A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1592A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2653A>G
  hgvsp: ENSP00000266022.4:p.Thr885Ala
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1087A>G
  hgvsp: ENSP00000392939.1:p.Thr363Ala
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*577A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*957A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.679A>G
  hgvsp: ENSP00000443165.1:p.Thr227Ala
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4773
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11113
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr885Ala
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

3-50102531-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102531
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102531
    reference: chr 3
allele count: 1
allele frequency: 8.245654540057389e-6
allele num: 121276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1593C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2654C>T
  hgvsp: ENSP00000266022.4:p.Thr885Ile
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1088C>T
  hgvsp: ENSP00000392939.1:p.Thr363Ile
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2258C>T
  hgvsp: ENSP00000396466.1:p.Thr753Ile
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*578C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*958C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.680C>T
  hgvsp: ENSP00000443165.1:p.Thr227Ile
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1088C>T
  hgvsp: ENSP00000393530.1:p.Thr363Ile
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*505C>T
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6830
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3142
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr885Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ

3-50102545-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102545
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102545
    reference: chr 3
allele count: 1
allele frequency: 8.256547442121603e-6
allele num: 121116
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2668G>A
  hgvsp: ENSP00000266022.4:p.Glu890Lys
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*519G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2272G>A
  hgvsp: ENSP00000396466.1:p.Glu758Lys
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.694G>A
  hgvsp: ENSP00000443165.1:p.Glu232Lys
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1102G>A
  hgvsp: ENSP00000393530.1:p.Glu368Lys
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*972G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*592G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1102G>A
  hgvsp: ENSP00000392939.1:p.Glu368Lys
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1607G>A
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6232
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2927
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Glu890Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff

3-50102547-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102547
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102547
    reference: chr 3
allele count: 2
allele frequency: 1.651636772041093e-5
allele num: 121092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*974G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.696G>A
  hgvsp: ENST00000539992.1:c.696G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*521G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1104G>A
  hgvsp: ENST00000422955.1:c.1104G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1609G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1104G>A
  hgvsp: ENST00000442092.1:c.1104G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*594G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2670G>A
  hgvsp: ENST00000266022.4:c.2670G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2274G>A
  hgvsp: ENST00000443081.1:c.2274G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6229
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3670
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4761
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5889
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1653
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2766
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu890Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

3-50102551-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102551
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102551
    reference: chr 3
allele count: 1
allele frequency: 8.26801600687899e-6
allele num: 120948
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1108C>T
  hgvsp: ENSP00000392939.1:p.Pro370Ser
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2278C>T
  hgvsp: ENSP00000396466.1:p.Pro760Ser
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1613C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*598C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1108C>T
  hgvsp: ENSP00000393530.1:p.Pro370Ser
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*525C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2674C>T
  hgvsp: ENSP00000266022.4:p.Pro892Ser
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.700C>T
  hgvsp: ENSP00000443165.1:p.Pro234Ser
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*978C>T
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6284
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6829
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4762
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1656
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro892Ser
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

http://identifiers.org/exac.variant/3-50102566-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102566
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102566
    reference: chr 3
allele count: 3
allele frequency: 2.494843989089216e-5
allele num: 120248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2286+7C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2682+7C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1116+7C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1621+7C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1116+7C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*986+7C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*533+7C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*606+7C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.708+7C>A
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5699
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6823
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9182
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
hgvs: c.2682+7C>A
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

3-50102573-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102573
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102573
    reference: chr 3
allele count: 14
allele frequency: 1.167698133351127e-4
allele num: 119894
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*986+14T>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1116+14T>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1621+14T>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1116+14T>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2682+14T>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*606+14T>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2286+14T>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*533+14T>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.708+14T>G
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6807
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6226
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5695
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 933
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5019
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5913
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6522
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3141
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

3-50102578-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102578
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102578
    reference: chr 3
allele count: 2
allele frequency: 1.671514057433223e-5
allele num: 119652
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1621+19C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*606+19C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2682+19C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.708+19C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2286+19C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*533+19C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*986+19C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1116+19C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1116+19C>T
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4748
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6520
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6786
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5694
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3140
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 873
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2900
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33338
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum

3-50102581-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102581
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102581
    reference: chr 3
allele count: 31
allele frequency: 2.593794973058001e-4
allele num: 119516
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*986+22T>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.708+22T>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1621+22T>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*533+22T>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2286+22T>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*606+22T>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2682+22T>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1116+22T>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1116+22T>G
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6778
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2576
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5693
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6517
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1978
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3668
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4758
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1997
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD

3-50102594-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102594
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102594
    reference: chr 3
allele count: 1
allele frequency: 8.403220113947665e-6
allele num: 119002
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*606+35G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2286+35G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1116+35G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*986+35G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2682+35G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1116+35G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1621+35G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*533+35G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.708+35G>A
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6742
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5962
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33317
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2634
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1444
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2712
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/3-50102598-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102598
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102598
    reference: chr 3
allele count: 2
allele frequency: 1.684891577227005e-5
allele num: 118702
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1116+39C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2682+39C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*986+39C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2286+39C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*606+39C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1621+39C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*533+39C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.708+39C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1116+39C>A
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6504
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6731
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5929
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3025
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3672
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2331
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: DP

3-50102599-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102599
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102599
    reference: chr 3
allele count: 48
allele frequency: 4.041288497482614e-4
allele num: 118774
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1621+40T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1116+40T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2682+40T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*986+40T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1116+40T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*606+40T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2286+40T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*533+40T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.708+40T>C
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5917
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5688
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6505
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6726
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4863
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3177
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3131
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1579
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

3-50102601-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102601
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102601
    reference: chr 3
allele count: 3
allele frequency: 2.527805864509606e-5
allele num: 118680
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*533+42G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.708+42G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*986+42G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2682+42G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1116+42G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*606+42G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2286+42G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1621+42G>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1116+42G>A
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2043
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5911
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 996
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5689
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3235
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6502
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2333
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3130
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1419
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1058
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

3-50102602-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102602
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102602
    reference: chr 3
allele count: 58
allele frequency: 4.893275963890998e-4
allele num: 118530
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1621+43G>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1116+43G>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2286+43G>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1116+43G>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*533+43G>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*606+43G>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.708+43G>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*986+43G>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2682+43G>C
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1977
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3222
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4757
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 6718
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5896
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1442
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4708
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 711
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2441
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3662
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5689
  bin: 5.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1693
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3126
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2584
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 632
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

3-50102604-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102604
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102604
    reference: chr 3
allele count: 1
allele frequency: 8.442808415791428e-6
allele num: 118444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1116+45A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2682+45A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1621+45A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*533+45A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*606+45A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1116+45A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*986+45A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2286+45A>G
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.708+45A>G
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1170
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4748
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3206
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3662
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5688
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1067
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2178
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2590
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

3-50102608-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102608
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102608
    reference: chr 3
allele count: 4
allele frequency: 3.385354954466976e-5
allele num: 118156
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*986+49T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*606+49T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1116+49T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1116+49T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*533+49T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2286+49T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1621+49T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2682+49T>C
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.708+49T>C
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4431
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3662
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1976
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5686
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6704
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3023
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5805
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6492
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2249
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 967
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2841
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

3-50102611-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102611
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102611
    reference: chr 3
allele count: 8
allele frequency: 6.790249202145719e-5
allele num: 117816
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*533+52C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*606+52C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1621+52C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*986+52C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1116+52C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1116+52C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.708+52C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2682+52C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2286+52C>T
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3662
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5685
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4748
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5792
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6687
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6490
  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1204
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1354
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2834
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2183
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1856
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum

3-50102965-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102965
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102965
    reference: chr 3
allele count: 1
allele frequency: 8.119519324455992e-5
allele num: 12316
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1116+406C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1622-47C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2286+406C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1116+406C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*606+406C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*533+406C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.708+406C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*986+406C>T
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2682+406C>T
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

http://identifiers.org/exac.variant/3-50102974-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 50102974
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 50102974
    reference: chr 3
allele count: 1
allele frequency: 8.119519324455992e-5
allele num: 12316
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000393530
  ensembl transcript: ENST00000442092
  gene symbol: RBM6
  hgvsc: ENST00000442092.1:c.1116+415C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000399942
  ensembl transcript: ENST00000434592
  gene symbol: RBM6
  hgvsc: ENST00000434592.1:c.*533+415C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000392939
  ensembl transcript: ENST00000422955
  gene symbol: RBM6
  hgvsc: ENST00000422955.1:c.1116+415C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000266022
  ensembl transcript: ENST00000266022
  gene symbol: RBM6
  hgvsc: ENST00000266022.4:c.2682+415C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000406548
  ensembl transcript: ENST00000454079
  gene symbol: RBM6
  hgvsc: ENST00000454079.1:c.*606+415C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396466
  ensembl transcript: ENST00000443081
  gene symbol: RBM6
  hgvsc: ENST00000443081.1:c.2286+415C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl transcript: ENST00000441115
  gene symbol: RBM6
  hgvsc: ENST00000441115.1:n.1622-38C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000396410
  ensembl transcript: ENST00000419610
  gene symbol: RBM6
  hgvsc: ENST00000419610.1:c.*986+415C>A
  variant of: http://identifiers.org/hgnc/9903
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000004534
  ensembl protein: ENSP00000443165
  ensembl transcript: ENST00000539992
  gene symbol: RBM6
  hgvsc: ENST00000539992.1:c.708+415C>A
  variant of: http://identifiers.org/hgnc/9903
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1952
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 494
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2130
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
reference allele: C

GenotypeQuality
all individuals: 21630
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 769
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3536
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1564
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2503
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2550
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 783
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17642
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1214
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5644
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 710
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5906
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7540
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13858
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.54e-1

MQ
type: SiteQuality
SIO_000300: 5.629e1

MQRankSum
type: SiteQuality
SIO_000300: 2.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.55e-1

QD
type: SiteQuality
SIO_000300: 6.12e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.55e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.739e0

DP
type: SiteQuality
SIO_000300: 1.096731e6

GenotypeQuality
all individuals: 1685
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2405
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 22054
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 832
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2601
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 487
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16988
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 650
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1193
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 1.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7360
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13736
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5588
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.640400194785072e-5
allele num: 45178
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.22e0

VQSLOD
type: SiteQuality
SIO_000300: -4.552e-1

QD
type: SiteQuality
SIO_000300: 1.552e1

MQ
type: SiteQuality
SIO_000300: 5.897e1

DP
type: SiteQuality
SIO_000300: 1.077836e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.64e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 480
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 970
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1137
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4462
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1023
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 471
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12413
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25261
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3432
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 410
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 796
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1768
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.906941266209001e-4
allele num: 5244
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42186
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5376
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7126
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6758
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.42e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e0

DP
type: SiteQuality
SIO_000300: 9.38231e5

MQ
type: SiteQuality
SIO_000300: 5.846e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.115e0

VQSLOD
type: SiteQuality
SIO_000300: -2.213e0

FS
type: SiteQuality
SIO_000300: 9.394e0

MQRankSum
type: SiteQuality
SIO_000300: -5.46e-1

QD
type: SiteQuality
SIO_000300: 4.44e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

GenotypeQuality
all individuals: 25922
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7134
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 795
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 520
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2049
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1511
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4484
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4627
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6579
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 299
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1069
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5056
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5734
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.003841844085161e-5
allele num: 12494
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4680
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

DP
type: SiteQuality
SIO_000300: 8.08567e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.77e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.327e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

QD
type: SiteQuality
SIO_000300: 7.18e0

GenotypeQuality
all individuals: 98
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1962
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1268
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4757
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2348
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5607
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 882
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25159
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1793
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 204
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 793
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 338
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4456
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.157937673356176e-5
allele num: 12258
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4980
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6380
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5282
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35414
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.71298e5

MQ
type: SiteQuality
SIO_000300: 5.813e1

MQRankSum
type: SiteQuality
SIO_000300: 8.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.91e0

QD
type: SiteQuality
SIO_000300: 1.732e1

VQSLOD
type: SiteQuality
SIO_000300: -3.896e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.969e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.78e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 118
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3160
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5240
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1252
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4598
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18730
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4384
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 263
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2262
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4472
bin: 1.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 6.942034015966679e-5
allele num: 28810
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3438
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11050
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3716
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4352
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.489e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.036e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.22e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.133e0

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

QD
type: SiteQuality
SIO_000300: 1.214e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.39e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

VQSLOD
type: SiteQuality
SIO_000300: 2.95e0

DP
type: SiteQuality
SIO_000300: 6.71157e5

GenotypeQuality
all individuals: 929
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1198
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3090
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.821753420469311e-5
allele num: 26166
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4056
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5060
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3122
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

QD
type: SiteQuality
SIO_000300: 6.95e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.45e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.279e0

DP
type: SiteQuality
SIO_000300: 6.56541e5

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

GenotypeQuality
all individuals: 534
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 135
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variant carriers: 0

GenotypeQuality
all individuals: 3221
bin: 8.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66172
num of homozygotes: 0

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

African
type: Population
allele count: 5
allele frequency: 4.829051574270813e-4
allele num: 10354
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.991209e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.23e-1

FS
type: SiteQuality
SIO_000300: 1.231e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-2

MQ
type: SiteQuality
SIO_000300: 5.925e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 8.76e0

GenotypeQuality
all individuals: 118
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 10891
bin: 9.75e1
variant carriers: 7

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 1573
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GenotypeQuality
all individuals: 496
bin: 2.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.020874241005347e-5
allele num: 66206
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.93012931866435e-4
allele num: 10362
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.476245654692932e-4
allele num: 8630
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.37e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.370000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.246e1

DP
type: SiteQuality
SIO_000300: 1.992356e6

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10885
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variant carriers: 1

GenotypeQuality
all individuals: 2272
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.641342074816814e-5
allele num: 10372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66368
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.858e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 7.34e-1

FS
type: SiteQuality
SIO_000300: 1.028e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.53e-1

DP
type: SiteQuality
SIO_000300: 1.999798e6

QD
type: SiteQuality
SIO_000300: 1.206e1

MQRankSum
type: SiteQuality
SIO_000300: 2.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7313
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66388
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.070171178827243e-5
allele num: 16474
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.000598e6

QD
type: SiteQuality
SIO_000300: 1.249e1

MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.47e-1

FS
type: SiteQuality
SIO_000300: 8.459e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.56e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505208019748329e-5
allele num: 66436
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.004096e6

QD
type: SiteQuality
SIO_000300: 1.413e1

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

FS
type: SiteQuality
SIO_000300: 7.681e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.47e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.991e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.041e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 287
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
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: 11568
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.025813827546783e-5
allele num: 66476
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-1

QD
type: SiteQuality
SIO_000300: 1.111e1

FS
type: SiteQuality
SIO_000300: 5.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.98e-1

DP
type: SiteQuality
SIO_000300: 2.004867e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.557e0

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 78
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GenotypeQuality
all individuals: 129
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GenotypeQuality
all individuals: 26962
bin: 6.25e1
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African
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East Asian
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num of homozygotes: 0

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

Other
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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 (Finnish)
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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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ReadPosRankSum
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MQ
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QD
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MQRankSum
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BaseQRankSum
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SIO_000300: -1.332e0

FS
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SIO_000300: 4.182e0

ClippingRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: 3.0e-4

DP
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SIO_000300: 2.006152e6

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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African
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allele frequency: 9.624639076034648e-5
allele num: 10390
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East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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VQSLOD
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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ClippingRankSum
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MQ
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BaseQRankSum
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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European (Finnish)
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South Asian
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African
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Latino
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InbreedingCoeff
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MQ
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ClippingRankSum
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VQSLOD
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DP
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

East Asian
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allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

Latino
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num of homozygotes: 0

South Asian
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QD
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FS
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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MQ
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BaseQRankSum
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DP
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SIO_000300: 2.008581e6

VQSLOD
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ClippingRankSum
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SIO_000300: 8.37e-1

GenotypeQuality
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variant carriers: 0

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

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

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

Other
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European (Non-Finnish)
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East Asian
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European (Finnish)
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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MQ
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MQRankSum
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DP
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QD
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ClippingRankSum
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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African
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European (Finnish)
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Other
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InbreedingCoeff
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QD
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MQRankSum
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ClippingRankSum
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MQ
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VQSLOD
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BaseQRankSum
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DP
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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East Asian
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African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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FS
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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QD
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MQRankSum
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VQSLOD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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Latino
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East Asian
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European (Non-Finnish)
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allele count: 6
allele frequency: 9.028530155290719e-5
allele num: 66456
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.622786759045419e-5
allele num: 10392
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

DP
type: SiteQuality
SIO_000300: 2.013619e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.02e-1

VQSLOD
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SIO_000300: 5.98e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

QD
type: SiteQuality
SIO_000300: 1.448e1

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505525277769414e-5
allele num: 66422
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10390
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East Asian
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.742e0

FS
type: SiteQuality
SIO_000300: 4.412e0

ClippingRankSum
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SIO_000300: -1.418e0

QD
type: SiteQuality
SIO_000300: 1.161e1

VQSLOD
type: SiteQuality
SIO_000300: 1.68e-1

MQ
type: SiteQuality
SIO_000300: 5.941e1

MQRankSum
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SIO_000300: -1.034e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 2.008819e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 908
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

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 count: 26
allele frequency: 2.503369921047564e-3
allele num: 10386
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66384
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

InbreedingCoeff
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SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.95e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.09e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.47e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

FS
type: SiteQuality
SIO_000300: 1.102e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.91e-1

QD
type: SiteQuality
SIO_000300: 1.219e1

DP
type: SiteQuality
SIO_000300: 2.008233e6

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66346
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
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

South Asian
type: Population
allele count: 1
allele frequency: 6.078288353999514e-5
allele num: 16452
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.32e-1

BaseQRankSum
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SIO_000300: 4.49e0

DP
type: SiteQuality
SIO_000300: 2.005838e6

QD
type: SiteQuality
SIO_000300: 1.126e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.957e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.765e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 1.83e0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66094
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.319109461966605e-4
allele num: 8624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.140997297961189e-5
allele num: 16284
num of homozygotes: 0

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

Other
type: Population
allele count: 0
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InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

ClippingRankSum
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SIO_000300: -1.4e-2

BaseQRankSum
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MQRankSum
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SIO_000300: -1.182e0

MQ
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 5.503e0

DP
type: SiteQuality
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ReadPosRankSum
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SIO_000300: -2.41e-1

QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.028100775193798e-5
allele num: 66048
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

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

East Asian
type: Population
allele count: 0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.504e0

ReadPosRankSum
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MQ
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QD
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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DP
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

African
type: Population
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allele frequency: 0.0e0
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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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allele num: 66018
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European (Finnish)
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VQSLOD
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DP
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MQ
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InbreedingCoeff
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MQRankSum
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FS
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QD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 1
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allele num: 65976
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Other
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East Asian
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European (Finnish)
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African
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Latino
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South Asian
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InbreedingCoeff
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QD
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FS
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ClippingRankSum
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MQ
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DP
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BaseQRankSum
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VQSLOD
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MQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
all individuals: 2228
bin: 9.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15684
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.52699731248473e-5
allele num: 65488
num of homozygotes: 0

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

VQSLOD
type: SiteQuality
SIO_000300: 5.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

FS
type: SiteQuality
SIO_000300: 2.207e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

MQ
type: SiteQuality
SIO_000300: 5.923e1

DP
type: SiteQuality
SIO_000300: 1.8807e6

GenotypeQuality
all individuals: 16
bin: 2.5e0
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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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503442884204829e-5
allele num: 66514
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10202
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 7.32e-1

MQ
type: SiteQuality
SIO_000300: 5.576e1

DP
type: SiteQuality
SIO_000300: 3.288192e6

ClippingRankSum
type: SiteQuality
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MQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: 1.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.11e-1

QD
type: SiteQuality
SIO_000300: 1.537e1

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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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503533303262667e-5
allele num: 66510
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10206
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.284e0

QD
type: SiteQuality
SIO_000300: 1.511e1

VQSLOD
type: SiteQuality
SIO_000300: -7.574e-1

DP
type: SiteQuality
SIO_000300: 3.289325e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.154e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.584e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.52e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 57
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variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.638562543192812e-5
allele num: 11576
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66526
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16212
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 9.66e-1

DP
type: SiteQuality
SIO_000300: 3.293372e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 6.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

QD
type: SiteQuality
SIO_000300: 1.581e1

MQ
type: SiteQuality
SIO_000300: 5.983e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.0e-3

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

GenotypeQuality
all individuals: 6
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 426
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GenotypeQuality
all individuals: 2611
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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
all individuals: 23
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2527
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GenotypeQuality
all individuals: 1522
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.509921828021648e-5
allele num: 66520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10218
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.3e0

DP
type: SiteQuality
SIO_000300: 3.295035e6

QD
type: SiteQuality
SIO_000300: 1.459e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.22e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.863e0

MQRankSum
type: SiteQuality
SIO_000300: -4.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
all individuals: 455
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 3180
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503216884132043e-5
allele num: 66524
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16224
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.815e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.877e0

FS
type: SiteQuality
SIO_000300: 6.739e0

VQSLOD
type: SiteQuality
SIO_000300: -6.532e-1

QD
type: SiteQuality
SIO_000300: 1.66e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.59e0

MQ
type: SiteQuality
SIO_000300: 5.941e1

DP
type: SiteQuality
SIO_000300: 3.295452e6

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 235
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GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16300
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502223290469895e-5
allele num: 66568
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.419e1

VQSLOD
type: SiteQuality
SIO_000300: 8.400000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.124e0

DP
type: SiteQuality
SIO_000300: 3.306729e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e-1

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 3

GenotypeQuality
all individuals: 9181
bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2744
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GenotypeQuality
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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: 1506
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GenotypeQuality
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GenotypeQuality
all individuals: 105
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GenotypeQuality
all individuals: 3112
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GenotypeQuality
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GenotypeQuality
all individuals: 2468
bin: 7.75e1
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GenotypeQuality
all individuals: 201
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 53
allele frequency: 5.849889624724062e-2
allele num: 906
num of homozygotes: 3

East Asian
type: Population
allele count: 242
allele frequency: 2.799629801018047e-2
allele num: 8644
num of homozygotes: 8

European (Finnish)
type: Population
allele count: 625
allele frequency: 9.449652252797097e-2
allele num: 6614
num of homozygotes: 23

South Asian
type: Population
allele count: 1757
allele frequency: 1.07435489788431e-1
allele num: 16354
num of homozygotes: 118

African
type: Population
allele count: 104
allele frequency: 1.005997291545753e-2
allele num: 10338
num of homozygotes: 0

Latino
type: Population
allele count: 292
allele frequency: 2.522460262612301e-2
allele num: 11576
num of homozygotes: 7

European (Non-Finnish)
type: Population
allele count: 4962
allele frequency: 7.449108268780399e-2
allele num: 66612
num of homozygotes: 189

QD
type: SiteQuality
SIO_000300: 1.493e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.73e-2

FS
type: SiteQuality
SIO_000300: 5.96e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
type: SiteQuality
SIO_000300: 3.767581e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.639999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.55e0

VQSLOD
type: SiteQuality
SIO_000300: 4.05e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.54e-1

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 2.25e1
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GenotypeQuality
all individuals: 33454
bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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European (Non-Finnish)
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DP
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VQSLOD
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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QD
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VQSLOD
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DP
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InbreedingCoeff
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MQ
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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South Asian
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DP
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MQRankSum
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VQSLOD
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InbreedingCoeff
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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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South Asian
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Latino
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African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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VQSLOD
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FS
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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East Asian
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Other
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South Asian
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European (Non-Finnish)
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FS
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QD
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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South Asian
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European (Finnish)
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MQ
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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FS
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VQSLOD
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QD
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DP
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Latino
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European (Finnish)
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African
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East Asian
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FS
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ClippingRankSum
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DP
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VQSLOD
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MQ
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InbreedingCoeff
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QD
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East Asian
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African
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European (Non-Finnish)
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InbreedingCoeff
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DP
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SIO_000300: 2.8604e6

VQSLOD
type: SiteQuality
SIO_000300: 8.62e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

GenotypeQuality
all individuals: 2766
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10861
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66612
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16396
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.45e-1

QD
type: SiteQuality
SIO_000300: 1.129e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.292e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.44e0

DP
type: SiteQuality
SIO_000300: 2.856871e6

FS
type: SiteQuality
SIO_000300: 4.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

GenotypeQuality
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bin: 6.75e1
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: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 93
bin: 2.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66600
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.91e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.545e0

QD
type: SiteQuality
SIO_000300: 1.428e1

MQ
type: SiteQuality
SIO_000300: 5.983e1

DP
type: SiteQuality
SIO_000300: 2.855786e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.581e0

GenotypeQuality
all individuals: 10510
bin: 6.25e1
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
all individuals: 1726
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GenotypeQuality
all individuals: 40
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50253929140247e-5
allele num: 66554
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.09e-1

FS
type: SiteQuality
SIO_000300: 2.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

DP
type: SiteQuality
SIO_000300: 2.852779e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.014e0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.85e-1

QD
type: SiteQuality
SIO_000300: 1.414e1

MQ
type: SiteQuality
SIO_000300: 5.972e1

GenotypeQuality
all individuals: 3141
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 16
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15854
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.595604775912787e-4
allele num: 11558
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66362
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.953e1

MQRankSum
type: SiteQuality
SIO_000300: -3.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.076e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.503e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.056e0

VQSLOD
type: SiteQuality
SIO_000300: 1.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.75e-1

DP
type: SiteQuality
SIO_000300: 2.834003e6

GenotypeQuality
all individuals: 1627
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 8002
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 14

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 2722
bin: 7.75e1
variant carriers: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.121076233183856e-3
allele num: 892
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 1.963212419583799e-4
allele num: 66218
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10330
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15692
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.14e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

FS
type: SiteQuality
SIO_000300: 4.413e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e-1

DP
type: SiteQuality
SIO_000300: 2.817671e6

VQSLOD
type: SiteQuality
SIO_000300: 9.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.78e-1

QD
type: SiteQuality
SIO_000300: 1.475e1

GenotypeQuality
all individuals: 33
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 119
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2718
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511807214344027e-5
allele num: 66146
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15568
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513775355737209e-4
allele num: 6606
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.527e1

VQSLOD
type: SiteQuality
SIO_000300: 9.18e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 2.807543e6

FS
type: SiteQuality
SIO_000300: 3.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -9.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.08e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 31

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6921
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 24
allele frequency: 3.631301821703081e-4
allele num: 66092
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11524
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.085402786190188e-4
allele num: 6604
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.699321047526673e-5
allele num: 10310
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15510
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.17e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

DP
type: SiteQuality
SIO_000300: 2.799539e6

QD
type: SiteQuality
SIO_000300: 1.478e1

GenotypeQuality
all individuals: 1706
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3138
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1000
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2871
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GenotypeQuality
all individuals: 1421
bin: 3.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65864
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.170138076293003e-4
allele num: 8546
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15310
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.36e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.769477e6

MQRankSum
type: SiteQuality
SIO_000300: -4.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.131e0

QD
type: SiteQuality
SIO_000300: 1.329e1

VQSLOD
type: SiteQuality
SIO_000300: 2.59e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

GenotypeQuality
all individuals: 33310
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1701
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GenotypeQuality
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GenotypeQuality
all individuals: 2577
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GenotypeQuality
all individuals: 176
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GenotypeQuality
all individuals: 462
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GenotypeQuality
all individuals: 1517
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GenotypeQuality
all individuals: 154
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1217
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5168
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2609
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1436
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2862
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1028
bin: 2.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.042102701387199e-5
allele num: 65744
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10284
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15158
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

FS
type: SiteQuality
SIO_000300: 3.291e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.97e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.656e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.95e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

QD
type: SiteQuality
SIO_000300: 1.421e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

DP
type: SiteQuality
SIO_000300: 2.76231e6

GenotypeQuality
all individuals: 2561
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1699
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2861
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1044
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 193
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1433
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
all individuals: 2612
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4839
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 33333
bin: 9.75e1
variant carriers: 45

GenotypeQuality
all individuals: 2329
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1311
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 240
bin: 7.5e0
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 47
allele frequency: 7.147419325405274e-4
allele num: 65758
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15220
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.703220191470844e-5
allele num: 11490
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.388e0

QD
type: SiteQuality
SIO_000300: 1.319e1

VQSLOD
type: SiteQuality
SIO_000300: 4.93e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.64e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.759371e6

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

GenotypeQuality
all individuals: 537
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1609
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2601
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 233
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2535
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33299
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2848
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4735
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8526
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15198
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.917152858809801e-4
allele num: 10284
num of homozygotes: 1

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

MQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.866e0

DP
type: SiteQuality
SIO_000300: 2.757338e6

ClippingRankSum
type: SiteQuality
SIO_000300: 9.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.31e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.909e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.24e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

GenotypeQuality
all individuals: 2205
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2419
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 909
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1440
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3989
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1401
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 33314
bin: 9.75e1
variant carriers: 58

GenotypeQuality
all individuals: 185
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1073
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1650
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2843
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 54
allele frequency: 5.253940455341506e-3
allele num: 10278
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15174
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.612330198537095e-4
allele num: 11484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524390243902439e-5
allele num: 65600
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.753745e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.87e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.16e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.786e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.91e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.58e-1

QD
type: SiteQuality
SIO_000300: 1.351e1

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeQuality
all individuals: 1641
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 985
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1457
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
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variant carriers: 0

GenotypeQuality
all individuals: 1694
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1397
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2413
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33285
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 640
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2842
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3970
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3133
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.612007405448295e-5
allele num: 15124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10274
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.12e0

MQRankSum
type: SiteQuality
SIO_000300: -7.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.223e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.4e-3

QD
type: SiteQuality
SIO_000300: 1.407e1

MQ
type: SiteQuality
SIO_000300: 5.912e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.751957e6

GenotypeQuality
all individuals: 2587
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3130
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1287
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1659
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1510
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1064
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1695
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1991
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33283
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 1377
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3072
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65448
num of homozygotes: 0

East Asian
type: Population
allele count: 4
allele frequency: 4.720320981826764e-4
allele num: 8474
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15032
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.53e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.659999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.51e-1

DP
type: SiteQuality
SIO_000300: 2.747305e6

FS
type: SiteQuality
SIO_000300: 6.153e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e0

QD
type: SiteQuality
SIO_000300: 1.528e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1043
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1319
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 644
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2495
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1509
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1656
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1687
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2578
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3126
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33269
bin: 9.75e1
variant carriers: 8

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8448
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14940
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.733624454148471e-5
allele num: 11450
num of homozygotes: 0

African
type: Population
allele count: 7
allele frequency: 6.847974955977304e-4
allele num: 10222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65284
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

FS
type: SiteQuality
SIO_000300: 6.403e0

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.91e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

QD
type: SiteQuality
SIO_000300: 1.511e1

DP
type: SiteQuality
SIO_000300: 2.746124e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.68e0

GenotypeQuality
all individuals: 507
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 738
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1970
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 307
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2139
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 55
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 5.319148936170213e-3
allele num: 188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7610
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.73e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.03e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.899e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.323e1

DP
type: SiteQuality
SIO_000300: 2.30245e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.82e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.46e-1

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1186
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 508
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 560
num of homozygotes: 0