3-28578589-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28578589
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 28578588
    reference: chr 3
allele count: 27
allele frequency: 3.994082840236687e-2
allele num: 676
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000206559
  ensembl protein: ENSP00000395421
  ensembl transcript: ENST00000457897
  gene symbol: ZCWPW2
  hgvsc: ENST00000457897.1:c.378-3delT
  variant of: http://identifiers.org/hgnc/23574
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 21
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 37
genotype depth: GenotypeDepth
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  bin: 2.5e0
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genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 42
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  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 229
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  variant carriers: 5
genotype quality: GenotypeQuality
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  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 9
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  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
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  variant carriers: 12
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 4
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4
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  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 21
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  variant carriers: 9
num of homozygotes: 0
population: African
  type: Population
  allele count: 13
  allele frequency: 1.048387096774194e-1
  allele num: 124
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 22
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10
  num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: AT
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

3-28578589-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28578589
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 28578590
    reference: chr 3
allele count: 9
allele frequency: 1.331360946745562e-2
allele num: 676
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000206559
  ensembl protein: ENSP00000395421
  ensembl transcript: ENST00000457897
  gene symbol: ZCWPW2
  hgvsc: ENST00000457897.1:c.378-3dupT
  variant of: http://identifiers.org/hgnc/23574
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
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  variant carriers: 2
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 124
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 22
  num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 6
  allele frequency: 1.818181818181818e-2
  allele num: 330
  num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

3-28578592-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28578592
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 28578592
    reference: chr 3
allele count: 6
allele frequency: 2.640845070422535e-3
allele num: 2272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000206559
  ensembl protein: ENSP00000395421
  ensembl transcript: ENST00000457897
  gene symbol: ZCWPW2
  hgvsc: ENST00000457897.1:c.378-10T>A
  variant of: http://identifiers.org/hgnc/23574
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
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genotype depth: GenotypeDepth
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  bin: 5.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 1
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 176
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
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  allele num: 48
  num of homozygotes: 0
population: Other
  type: Population
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  allele num: 38
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

3-28578594-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28578594
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 28578594
    reference: chr 3
allele count: 1
allele frequency: 4.233700254022015e-4
allele num: 2362
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000206559
  ensembl protein: ENSP00000395421
  ensembl transcript: ENST00000457897
  gene symbol: ZCWPW2
  hgvsc: ENST00000457897.1:c.378-8T>A
  variant of: http://identifiers.org/hgnc/23574
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: c.378-8T>A
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 1
  allele frequency: 9.09090909090909e-3
  allele num: 110
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1232
  num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

3-28578605-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28578605
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 28578606
    reference: chr 3
allele count: 174
allele frequency: 1.614100185528757e-1
allele num: 1078
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000206559
  ensembl protein: ENSP00000395421
  ensembl transcript: ENST00000457897
  gene symbol: ZCWPW2
  hgvsc: ENST00000457897.1:c.392dupT
  hgvsp: ENSP00000395421.1:p.Gly132TrpfsTer3
  variant of: http://identifiers.org/hgnc/23574
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 151
genotype depth: GenotypeDepth
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  variant carriers: 135
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 1.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 36
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 24
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 48
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 7.5e0
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 6.75e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 3653
  bin: 2.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 2.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 1.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 44
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 8.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 6.25e1
  variant carriers: 20
hgvs: p.Gly132TrpfsTer3
num of homozygotes: 1
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 7
  allele frequency: 1.75e-1
  allele num: 40
  num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-28578605-A-ATT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28578605
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 28578607
    reference: chr 3
allele count: 2
allele frequency: 1.855287569573284e-3
allele num: 1078
alternate allele: ATT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000206559
  ensembl protein: ENSP00000395421
  ensembl transcript: ENST00000457897
  gene symbol: ZCWPW2
  hgvsc: ENST00000457897.1:c.391_392dupTT
  hgvsp: ENSP00000395421.1:p.Gly132LeufsTer15
  variant of: http://identifiers.org/hgnc/23574
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3653
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 187
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly132LeufsTer15
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 24
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 66
  num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

3-28578605-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28578605
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 28578605
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 1078
alternate allele: T
canonical: false
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 700
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 3653
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 51
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  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 66
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 24
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: NaN
  allele num: 0
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 10
  num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

3-28578605-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28578605
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 28578604
    reference: chr 3
allele count: 98
allele frequency: 9.090909090909091e-2
allele num: 1078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000206559
  ensembl protein: ENSP00000395421
  ensembl transcript: ENST00000457897
  gene symbol: ZCWPW2
  hgvsc: ENST00000457897.1:c.392delT
  hgvsp: ENSP00000395421.1:p.Phe131LeufsTer15
  variant of: http://identifiers.org/hgnc/23574
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 2.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2686
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  variant carriers: 47
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
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  variant carriers: 78
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
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  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 57
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  variant carriers: 21
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3653
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 70
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3
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  variant carriers: 2
hgvs: p.Phe131LeufsTer15
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 22
  allele frequency: 7.096774193548387e-2
  allele num: 310
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: NaN
  allele num: 0
  num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: AT
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

3-28578606-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28578606
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 28578606
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 666
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000206559
  ensembl protein: ENSP00000395421
  ensembl transcript: ENST00000457897
  gene symbol: ZCWPW2
  hgvsc: ENST00000457897.1:c.382T>A
  hgvsp: ENSP00000395421.1:p.Ile128Asn
  variant of: http://identifiers.org/hgnc/23574
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
hgvs: p.Ile128Asn
num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: NaN
  allele num: 0
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 14
  num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

3-28578611-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28578611
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 28578611
    reference: chr 3
allele count: 3
allele frequency: 6.284038542103058e-4
allele num: 4774
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000206559
  ensembl protein: ENSP00000395421
  ensembl transcript: ENST00000457897
  gene symbol: ZCWPW2
  hgvsc: ENST00000457897.1:c.387T>G
  hgvsp: ENSP00000395421.1:p.Phe130Val
  variant of: http://identifiers.org/hgnc/23574
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1732
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2175
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 663
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1715
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 55
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 506
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genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Phe130Val
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 64
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 3
  allele frequency: 9.322560596643878e-4
  allele num: 3218
  num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD

3-28578622-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28578622
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 28578623
    reference: chr 3
allele count: 3
allele frequency: 5.880047040376323e-4
allele num: 5102
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000206559
  ensembl protein: ENSP00000395421
  ensembl transcript: ENST00000457897
  gene symbol: ZCWPW2
  hgvsc: ENST00000457897.1:c.399dupA
  hgvsp: ENSP00000395421.1:p.Arg134LysfsTer11
  variant of: http://identifiers.org/hgnc/23574
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1692
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1845
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  variant carriers: 2
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1623
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2693
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 450
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 91
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
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  variant carriers: 0
hgvs: p.Arg134LysfsTer11
num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 48
  num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 58
  num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-28578628-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28578628
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 28578628
    reference: chr 3
allele count: 1
allele frequency: 1.731301939058172e-4
allele num: 5776
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000206559
  ensembl protein: ENSP00000395421
  ensembl transcript: ENST00000457897
  gene symbol: ZCWPW2
  hgvsc: ENST00000457897.1:c.404C>G
  hgvsp: ENST00000457897.1:c.404C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23574
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 10
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  variant carriers: 0
hgvs: p.Val135Val
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 66
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 128
  num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-28578720-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28578720
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 28578720
    reference: chr 3
allele count: 1
allele frequency: 1.887504718761797e-4
allele num: 5298
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000206559
  ensembl protein: ENSP00000395421
  ensembl transcript: ENST00000457897
  gene symbol: ZCWPW2
  hgvsc: ENST00000457897.1:c.496C>T
  hgvsp: ENSP00000395421.1:p.Pro166Leu
  variant of: http://identifiers.org/hgnc/23574
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 2173
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2
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genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
hgvs: p.Pro166Leu
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 2.698327037236913e-4
  allele num: 3706
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 52
  num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

3-28579341-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28579341
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 28579341
    reference: chr 3
allele count: 1
allele frequency: 7.121492664862555e-5
allele num: 14042
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000206559
  ensembl protein: ENSP00000395421
  ensembl transcript: ENST00000457897
  gene symbol: ZCWPW2
  hgvsc: ENST00000457897.1:c.519-32A>G
  variant of: http://identifiers.org/hgnc/23574
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1696
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3103
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 7556
  num of homozygotes: 0
population: Latino
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 188
  num of homozygotes: 0
population: European (Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 1558
  num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-28579390-GTT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28579390
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 28579388
    reference: chr 3
allele count: 1
allele frequency: 6.945409084595083e-5
allele num: 14398
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000206559
  ensembl protein: ENSP00000395421
  ensembl transcript: ENST00000457897
  gene symbol: ZCWPW2
  hgvsc: ENST00000457897.1:c.538_539delTT
  hgvsp: ENSP00000395421.1:p.Phe180TyrfsTer5
  variant of: http://identifiers.org/hgnc/23574
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 501
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3975
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 367
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 569
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Phe180TyrfsTer5
num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 1.313025210084034e-4
  allele num: 7616
  num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 586
  num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: GTT
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD

3-28579395-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28579395
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 28579395
    reference: chr 3
allele count: 6
allele frequency: 4.165509580672035e-4
allele num: 14404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000206559
  ensembl protein: ENSP00000395421
  ensembl transcript: ENST00000457897
  gene symbol: ZCWPW2
  hgvsc: ENST00000457897.1:c.541T>C
  hgvsp: ENSP00000395421.1:p.Met181Thr
  variant of: http://identifiers.org/hgnc/23574
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3203
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1474
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2400
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3975
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 367
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1345
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1160
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.25e1
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genotype quality: GenotypeQuality
  all individuals: 484
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genotype quality: GenotypeQuality
  all individuals: 566
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Met181Thr
num of homozygotes: 0
population: Other
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 184
  num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 198
  num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

3-28579429-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28579429
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 28579429
    reference: chr 3
allele count: 1
allele frequency: 6.955070246209486e-5
allele num: 14378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  ensembl gene: ENSG00000206559
  ensembl protein: ENSP00000395421
  ensembl transcript: ENST00000457897
  gene symbol: ZCWPW2
  hgvsc: ENST00000457897.1:c.575G>A
  hgvsp: ENST00000457897.1:c.575G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23574
canonical: false
consequence: stop retained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2401
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1427
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3879
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 138
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 173
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 141
  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 362
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ter192Ter
num of homozygotes: 0
population: European (Non-Finnish)
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 4026
  num of homozygotes: 0
population: South Asian
  type: Population
  allele count: 1
  allele frequency: 1.312680493567866e-4
  allele num: 7618
  num of homozygotes: 0
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/3-29323122-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323122
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323122
    reference: chr 3
allele count: 1
allele frequency: 8.302613662781043e-6
allele num: 120444
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.-51A>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.-51A>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.-51A>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.-51A>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.-51A>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.449A>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.-51A>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+9047T>G
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.-51A>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.-51A>C
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5430
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3029
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12596
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3773
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11182
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8166
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20164
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum

3-29323123-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323123
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323123
    reference: chr 3
allele count: 1
allele frequency: 8.301924386072691e-6
allele num: 120454
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.-50C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.-50C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.-50C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.-50C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.450C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.-50C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.-50C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.-50C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.-50C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+9046G>A
  variant of: http://identifiers.org/hgnc/39989
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12601
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8174
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5749
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3296
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

3-29323130-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323130
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323130
    reference: chr 3
allele count: 5
allele frequency: 4.148207144871987e-5
allele num: 120534
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.457C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.-43C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.-43C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.-43C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.-43C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.-43C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.-43C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.-43C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.-43C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+9039G>A
  variant of: http://identifiers.org/hgnc/39989
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9901
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5448
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8235
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3034
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11507
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11757
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

3-29323134-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323134
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323134
    reference: chr 3
allele count: 7
allele frequency: 5.804408033300718e-5
allele num: 120598
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.-39C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+9035G>A
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.-39C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.-39C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.-39C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.-39C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.461C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.-39C>T
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8248
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5456
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4885
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

3-29323138-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323138
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323138
    reference: chr 3
allele count: 1
allele frequency: 8.287475966319697e-6
allele num: 120664
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.-35C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+9031G>C
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.-35C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.-35C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.465C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.-35C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.-35C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.-35C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.-35C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.-35C>G
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11811
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8274
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3412
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2553
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

3-29323139-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323139
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323139
    reference: chr 3
allele count: 4
allele frequency: 3.314056570945666e-5
allele num: 120698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.-34A>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.-34A>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.-34A>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.-34A>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+9030T>A
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.-34A>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.466A>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.-34A>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.-34A>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.-34A>T
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13258
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10935
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11808
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

3-29323141-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323141
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323141
    reference: chr 3
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.-32T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.-32T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+9028A>G
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.468T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.-32T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.-32T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.-32T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.-32T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.-32T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.-32T>C
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11846
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5466
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13310
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/3-29323148-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323148
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323148
    reference: chr 3
allele count: 1
allele frequency: 8.273762245168123e-6
allele num: 120864
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.-25C>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.-25C>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.-25C>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.-25C>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.-25C>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.-25C>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.475C>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+9021G>T
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.-25C>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.-25C>A
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5470
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8315
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3452
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ

3-29323151-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323151
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323151
    reference: chr 3
allele count: 1
allele frequency: 8.271024945411235e-6
allele num: 120904
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.-22C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.-22C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.-22C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+9018G>A
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.-22C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.-22C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.-22C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.478C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.-22C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.-22C>T
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11244
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11973
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8320
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4649
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ

3-29323152-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323152
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323152
    reference: chr 3
allele count: 2
allele frequency: 1.654013463669594e-5
allele num: 120918
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.-21G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.-21G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.-21G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.-21G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.-21G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.-21G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.-21G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.-21G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+9017C>T
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.479G>A
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11994
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3948
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3454
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

3-29323155-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323155
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323155
    reference: chr 3
allele count: 1
allele frequency: 8.265965712774223e-6
allele num: 120978
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.-18G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.-18G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.-18G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+9014C>G
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.-18G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.-18G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.-18G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.-18G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.482G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.-18G>C
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12000
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8321
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13668
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3463
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ

3-29323157-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323157
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323157
    reference: chr 3
allele count: 1
allele frequency: 8.264872638312644e-6
allele num: 120994
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.-16T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.-16T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.-16T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.-16T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.-16T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.-16T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.484T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.-16T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.-16T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+9012A>G
  variant of: http://identifiers.org/hgnc/39989
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2562
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD

3-29323157-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323157
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323157
    reference: chr 3
allele count: 4
allele frequency: 3.305949055325058e-5
allele num: 120994
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.-16T>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.-16T>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.-16T>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.-16T>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.484T>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.-16T>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.-16T>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.-16T>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+9012A>C
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.-16T>G
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3044
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11232
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2562
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4656
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP

3-29323168-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323168
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323168
    reference: chr 3
allele count: 1
allele frequency: 8.260366760284156e-6
allele num: 121060
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.-5G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.-5G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.-5G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.-5G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.-5G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.495G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.-5G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.-5G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+9001C>A
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.-5G>T
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8325
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3476
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

3-29323180-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323180
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323180
    reference: chr 3
allele count: 1
allele frequency: 8.25559316436886e-6
allele num: 121130
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.8A>G
  hgvsp: ENSP00000273139.9:p.Lys3Arg
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.8A>G
  hgvsp: ENSP00000400519.1:p.Lys3Arg
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.8A>G
  hgvsp: ENSP00000379828.3:p.Lys3Arg
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.8A>G
  hgvsp: ENSP00000395592.1:p.Lys3Arg
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.8A>G
  hgvsp: ENSP00000373276.2:p.Lys3Arg
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+8989T>C
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.8A>G
  hgvsp: ENSP00000397926.1:p.Lys3Arg
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.8A>G
  hgvsp: ENSP00000391934.1:p.Lys3Arg
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.8A>G
  hgvsp: ENSP00000373277.2:p.Lys3Arg
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.507A>G
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13808
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8327
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Lys3Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-29323182-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323182
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323182
    reference: chr 3
allele count: 1
allele frequency: 8.255047961828658e-6
allele num: 121138
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.509C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.10C>T
  hgvsp: ENSP00000397926.1:p.Arg4Cys
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.10C>T
  hgvsp: ENSP00000373276.2:p.Arg4Cys
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.10C>T
  hgvsp: ENSP00000391934.1:p.Arg4Cys
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.10C>T
  hgvsp: ENSP00000395592.1:p.Arg4Cys
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.10C>T
  hgvsp: ENSP00000379828.3:p.Arg4Cys
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.10C>T
  hgvsp: ENSP00000400519.1:p.Arg4Cys
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.10C>T
  hgvsp: ENSP00000273139.9:p.Arg4Cys
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.10C>T
  hgvsp: ENSP00000373277.2:p.Arg4Cys
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+8987G>A
  variant of: http://identifiers.org/hgnc/39989
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5483
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12023
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3477
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg4Cys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: QD

3-29323214-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323214
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323214
    reference: chr 3
allele count: 1
allele frequency: 8.251642076773278e-6
allele num: 121188
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.42C>T
  hgvsp: ENST00000396583.3:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.42C>T
  hgvsp: ENST00000445033.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.42C>T
  hgvsp: ENST00000383766.2:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.42C>T
  hgvsp: ENST00000434693.2:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+8955G>A
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.541C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.42C>T
  hgvsp: ENST00000452462.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.42C>T
  hgvsp: ENST00000456853.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.42C>T
  hgvsp: ENST00000383767.2:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.42C>T
  hgvsp: ENST00000273139.9:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13858
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5480
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6224
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3951
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Tyr14Tyr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/3-29323216-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323216
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323216
    reference: chr 3
allele count: 2
allele frequency: 1.650355651642929e-5
allele num: 121186
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.44C>A
  hgvsp: ENSP00000373277.2:p.Thr15Asn
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.44C>A
  hgvsp: ENSP00000379828.3:p.Thr15Asn
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.543C>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.44C>A
  hgvsp: ENSP00000397926.1:p.Thr15Asn
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.44C>A
  hgvsp: ENSP00000273139.9:p.Thr15Asn
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.44C>A
  hgvsp: ENSP00000400519.1:p.Thr15Asn
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+8953G>T
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.44C>A
  hgvsp: ENSP00000395592.1:p.Thr15Asn
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.44C>A
  hgvsp: ENSP00000373276.2:p.Thr15Asn
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.44C>A
  hgvsp: ENSP00000391934.1:p.Thr15Asn
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 721
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13856
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr15Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

3-29323229-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323229
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323229
    reference: chr 3
allele count: 1
allele frequency: 8.253957772752034e-6
allele num: 121154
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.57T>G
  hgvsp: ENST00000456853.1:c.57T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.57T>G
  hgvsp: ENST00000273139.9:c.57T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.57T>G
  hgvsp: ENST00000445033.1:c.57T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.57T>G
  hgvsp: ENST00000396583.3:c.57T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.57T>G
  hgvsp: ENST00000383766.2:c.57T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.556T>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.57T>G
  hgvsp: ENST00000434693.2:c.57T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+8940A>C
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.57T>G
  hgvsp: ENST00000383767.2:c.57T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.57T>G
  hgvsp: ENST00000452462.1:c.57T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11154
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13855
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14287
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro19Pro
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

3-29323235-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323235
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323235
    reference: chr 3
allele count: 1
allele frequency: 8.254911672445104e-6
allele num: 121140
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.562T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.63T>C
  hgvsp: ENST00000383766.2:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.63T>C
  hgvsp: ENST00000273139.9:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.63T>C
  hgvsp: ENST00000434693.2:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.63T>C
  hgvsp: ENST00000456853.1:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.63T>C
  hgvsp: ENST00000445033.1:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.63T>C
  hgvsp: ENST00000452462.1:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+8934A>G
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.63T>C
  hgvsp: ENST00000383767.2:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.63T>C
  hgvsp: ENST00000396583.3:c.63T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8322
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5479
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13852
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12027
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Tyr21Tyr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum

3-29323250-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323250
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323250
    reference: chr 3
allele count: 1
allele frequency: 8.258593066085262e-6
allele num: 121086
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.75+3A>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.75+3A>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.75+3A>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.75+3A>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.75+3A>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.75+3A>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+8919T>A
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.574+3A>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.75+3A>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.75+3A>T
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11991
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8313
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3046
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3952
  bin: 9.25e1
  variant carriers: 0
hgvs: c.75+3A>T
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

3-29323263-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323263
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323263
    reference: chr 3
allele count: 1
allele frequency: 8.266239026567692e-6
allele num: 120974
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.75+16C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.75+16C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.75+16C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.75+16C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.75+16C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.75+16C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.574+16C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+8906G>A
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.75+16C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.75+16C>T
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11887
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8301
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3052
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6108
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13724
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3937
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

3-29323264-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323264
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323264
    reference: chr 3
allele count: 1
allele frequency: 8.265965712774223e-6
allele num: 120978
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.75+17G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.75+17G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+8905C>A
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.574+17G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.75+17G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.75+17G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.75+17G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.75+17G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.75+17G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.75+17G>T
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8306
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5458
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13706
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3937
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3447
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

3-29323267-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323267
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323267
    reference: chr 3
allele count: 2
allele frequency: 1.653247805313538e-5
allele num: 120974
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+8902G>A
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.75+20C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.75+20C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.574+20C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.75+20C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.75+20C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.75+20C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.75+20C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.75+20C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.75+20C>T
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11820
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5457
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1711
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8297
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3432
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6082
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20262
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

3-29323271-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323271
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323271
    reference: chr 3
allele count: 5
allele frequency: 4.135102054318701e-5
allele num: 120916
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+8898G>C
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.75+24C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.75+24C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.75+24C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.75+24C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.574+24C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.75+24C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.75+24C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.75+24C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.75+24C>G
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 832
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3049
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10740
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11775
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13507
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13285
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4996
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2563
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

3-29323272-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323272
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323272
    reference: chr 3
allele count: 1
allele frequency: 8.269246671628215e-6
allele num: 120930
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+8897C>T
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.75+25G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.75+25G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.75+25G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.75+25G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.75+25G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.75+25G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.75+25G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.574+25G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.75+25G>A
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20256
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

3-29323277-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323277
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323277
    reference: chr 3
allele count: 1
allele frequency: 8.270067318347971e-6
allele num: 120918
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.75+30G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.574+30G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.75+30G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.75+30G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.75+30G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.75+30G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.75+30G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.75+30G>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+8892C>A
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.75+30G>T
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5442
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10600
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2561
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4608
  bin: 8.25e1
  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: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

3-29323287-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323287
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323287
    reference: chr 3
allele count: 9
allele frequency: 7.447125409591897e-5
allele num: 120852
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.75+40G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+8882C>G
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.574+40G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.75+40G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.75+40G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.75+40G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.75+40G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.75+40G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.75+40G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.75+40G>C
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5437
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12743
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11456
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11916
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

3-29323291-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323291
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323291
    reference: chr 3
allele count: 1
allele frequency: 8.275268532463878e-6
allele num: 120842
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.75+44T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.75+44T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.574+44T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.75+44T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.75+44T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.75+44T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+8878A>G
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.75+44T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.75+44T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.75+44T>C
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11406
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 840
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 363
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4909
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

3-29323291-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29323291
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29323291
    reference: chr 3
allele count: 13
allele frequency: 1.075784909220304e-4
allele num: 120842
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.574+44T>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.75+44T>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.75+44T>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.75+44T>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.75+44T>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000235904
  ensembl transcript: ENST00000413430
  gene symbol: RBMS3-AS3
  hgvsc: ENST00000413430.1:n.49+8878A>C
  variant of: http://identifiers.org/hgnc/39989
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.75+44T>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.75+44T>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.75+44T>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.75+44T>G
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5435
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1099
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3045
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11406
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8260
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5746
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

3-29476183-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476183
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476183
    reference: chr 3
allele count: 1
allele frequency: 8.809486054583575e-6
allele num: 113514
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.76-51T>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.575-51T>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.76-54T>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.76-54T>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.76-51T>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.76-51T>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.76-51T>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.76-51T>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.76-51T>A
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3369
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3096
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4513
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4308
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4976
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1061
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1728
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1120
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1796
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 879
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

3-29476186-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476186
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476186
    reference: chr 3
allele count: 3
allele frequency: 2.643684238354571e-5
allele num: 113478
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.76-48A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.76-48A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.76-48A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.575-48A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.76-51A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.76-48A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.76-48A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.76-51A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.76-48A>G
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1610
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5032
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3371
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4513
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4999
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5424
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2003
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

3-29476188-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476188
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476188
    reference: chr 3
allele count: 827
allele frequency: 7.288655432560107e-3
allele num: 113464
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.76-46A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.76-46A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.76-46A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.76-46A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.575-46A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.76-46A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.76-46A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.76-49A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.76-49A>G
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1628
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 746
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2511
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3086
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3906
  bin: 7.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 3367
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 6.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 7.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 5.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 8.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 9.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 5423
  bin: 5.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 8.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 4969
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 4513
  bin: 6.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 9.75e1
  variant carriers: 445
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1219
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1722
  bin: 8.25e1
  variant carriers: 2
num of homozygotes: 32
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

3-29476189-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476189
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476189
    reference: chr 3
allele count: 63
allele frequency: 5.548509828788839e-4
allele num: 113544
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.76-45G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.575-45G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.76-45G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.76-45G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.76-45G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.76-48G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.76-45G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.76-48G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.76-45G>C
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3921
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4527
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 9.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5030
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2556
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5471
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5168
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1248
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1744
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP

3-29476196-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476196
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476196
    reference: chr 3
allele count: 1
allele frequency: 8.787346221441125e-6
allele num: 113800
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.76-38G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.575-38G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.76-38G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.76-38G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.76-38G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.76-38G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.76-41G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.76-38G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.76-41G>C
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5035
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5175
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4367
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1416
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4616
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 904
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

3-29476216-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476216
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476216
    reference: chr 3
allele count: 4
allele frequency: 3.469090404495941e-5
allele num: 115304
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.76-18A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.76-18A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.76-18A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.76-18A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.76-21A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.575-18A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.76-18A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.76-18A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.76-21A>G
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1344
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3248
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1146
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2584
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

3-29476217-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476217
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476217
    reference: chr 3
allele count: 1
allele frequency: 8.667464073361416e-6
allele num: 115374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.76-20G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.575-17G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.76-17G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.76-20G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.76-17G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.76-17G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.76-17G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.76-17G>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.76-17G>C
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1751
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44649
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1147
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

3-29476226-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476226
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476226
    reference: chr 3
allele count: 1
allele frequency: 8.576476440419219e-6
allele num: 116598
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.76-8G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.76-8G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.76-8G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.76-8G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.76-8G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.76-11G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.575-8G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.76-11G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.76-8G>A
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5033
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 924
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
hgvs: c.76-8G>A
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

3-29476230-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476230
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476230
    reference: chr 3
allele count: 15
allele frequency: 1.278358247115171e-4
allele num: 117338
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.76-4C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.76-7C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.76-4C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.76-4C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.575-4C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.76-4C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.76-4C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.76-7C>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.76-4C>G
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4613
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4368
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5476
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1885
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 3.25e1
  variant carriers: 0
hgvs: c.76-4C>G
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

3-29476231-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476231
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476231
    reference: chr 3
allele count: 1
allele frequency: 8.500943604740126e-6
allele num: 117634
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.76-3C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.76-3C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.76-3C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.575-3C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.76-3C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.76-3C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.76-3C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.76-6C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.76-6C>T
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4370
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2661
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3442
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4606
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44643
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1442
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
hgvs: c.76-3C>T
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ

3-29476238-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476238
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476238
    reference: chr 3
allele count: 2
allele frequency: 1.682481997442627e-5
allele num: 118872
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.80C>T
  hgvsp: ENSP00000400519.1:p.Ser27Phe
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.80C>T
  hgvsp: ENSP00000397926.1:p.Ser27Phe
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.77C>T
  hgvsp: ENSP00000395592.1:p.Ser26Phe
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.80C>T
  hgvsp: ENSP00000379828.3:p.Ser27Phe
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.80C>T
  hgvsp: ENSP00000391934.1:p.Ser27Phe
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.77C>T
  hgvsp: ENSP00000373276.2:p.Ser26Phe
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.80C>T
  hgvsp: ENSP00000373277.2:p.Ser27Phe
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.579C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.80C>T
  hgvsp: ENSP00000273139.9:p.Ser27Phe
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4378
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5035
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2729
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2008
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3473
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4605
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1414
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2037
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44644
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Ser27Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

3-29476251-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476251
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476251
    reference: chr 3
allele count: 18
allele frequency: 1.494768310911809e-4
allele num: 120420
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.93T>C
  hgvsp: ENST00000445033.1:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.93T>C
  hgvsp: ENST00000456853.1:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.93T>C
  hgvsp: ENST00000383767.2:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.93T>C
  hgvsp: ENST00000273139.9:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.93T>C
  hgvsp: ENST00000452462.1:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.90T>C
  hgvsp: ENST00000434693.2:c.90T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.90T>C
  hgvsp: ENST00000383766.2:c.90T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.592T>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.93T>C
  hgvsp: ENST00000396583.3:c.93T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5034
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3247
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4539
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4603
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5478
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2040
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala31Ala
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD

3-29476252-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476252
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476252
    reference: chr 3
allele count: 1
allele frequency: 8.295037908323241e-6
allele num: 120554
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.94C>T
  hgvsp: ENSP00000400519.1:p.Pro32Ser
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.94C>T
  hgvsp: ENSP00000273139.9:p.Pro32Ser
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.94C>T
  hgvsp: ENSP00000391934.1:p.Pro32Ser
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.593C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.94C>T
  hgvsp: ENSP00000373277.2:p.Pro32Ser
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.91C>T
  hgvsp: ENSP00000373276.2:p.Pro31Ser
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.91C>T
  hgvsp: ENSP00000395592.1:p.Pro31Ser
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.94C>T
  hgvsp: ENSP00000379828.3:p.Pro32Ser
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.94C>T
  hgvsp: ENSP00000397926.1:p.Pro32Ser
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3932
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4390
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5180
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44643
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Pro32Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff

3-29476253-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476253
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476253
    reference: chr 3
allele count: 1
allele frequency: 8.29228651508367e-6
allele num: 120594
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.95C>T
  hgvsp: ENSP00000373277.2:p.Pro32Leu
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.95C>T
  hgvsp: ENSP00000391934.1:p.Pro32Leu
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.95C>T
  hgvsp: ENSP00000379828.3:p.Pro32Leu
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.95C>T
  hgvsp: ENSP00000273139.9:p.Pro32Leu
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.92C>T
  hgvsp: ENSP00000395592.1:p.Pro31Leu
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.95C>T
  hgvsp: ENSP00000400519.1:p.Pro32Leu
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.95C>T
  hgvsp: ENSP00000397926.1:p.Pro32Leu
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.92C>T
  hgvsp: ENSP00000373276.2:p.Pro31Leu
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.594C>T
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4541
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5179
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2007
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3499
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4384
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2038
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro32Leu
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

3-29476255-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476255
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476255
    reference: chr 3
allele count: 2
allele frequency: 1.657000828500414e-5
allele num: 120700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.97C>T
  hgvsp: ENSP00000391934.1:p.His33Tyr
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.97C>T
  hgvsp: ENSP00000400519.1:p.His33Tyr
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.94C>T
  hgvsp: ENSP00000373276.2:p.His32Tyr
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.97C>T
  hgvsp: ENSP00000273139.9:p.His33Tyr
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.94C>T
  hgvsp: ENSP00000395592.1:p.His32Tyr
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.97C>T
  hgvsp: ENSP00000373277.2:p.His33Tyr
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.97C>T
  hgvsp: ENSP00000379828.3:p.His33Tyr
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.97C>T
  hgvsp: ENSP00000397926.1:p.His33Tyr
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.596C>T
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3244
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3043
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3931
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5481
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5038
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
hgvs: p.His33Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/3-29476256-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476256
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476256
    reference: chr 3
allele count: 2
allele frequency: 1.656534199148542e-5
allele num: 120734
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.98A>C
  hgvsp: ENSP00000373277.2:p.His33Pro
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.98A>C
  hgvsp: ENSP00000400519.1:p.His33Pro
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.98A>C
  hgvsp: ENSP00000379828.3:p.His33Pro
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.98A>C
  hgvsp: ENSP00000391934.1:p.His33Pro
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.95A>C
  hgvsp: ENSP00000373276.2:p.His32Pro
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.98A>C
  hgvsp: ENSP00000273139.9:p.His33Pro
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.95A>C
  hgvsp: ENSP00000395592.1:p.His32Pro
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.98A>C
  hgvsp: ENSP00000397926.1:p.His33Pro
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.597A>C
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4601
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5479
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3505
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2594
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2005
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1592
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1798
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44628
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His33Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ

3-29476267-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476267
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476267
    reference: chr 3
allele count: 2
allele frequency: 1.65180046250413e-5
allele num: 121080
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.109C>T
  hgvsp: ENSP00000391934.1:p.Pro37Ser
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.109C>T
  hgvsp: ENSP00000400519.1:p.Pro37Ser
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.608C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.109C>T
  hgvsp: ENSP00000379828.3:p.Pro37Ser
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.109C>T
  hgvsp: ENSP00000273139.9:p.Pro37Ser
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.106C>T
  hgvsp: ENSP00000395592.1:p.Pro36Ser
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.109C>T
  hgvsp: ENSP00000397926.1:p.Pro37Ser
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.106C>T
  hgvsp: ENSP00000373276.2:p.Pro36Ser
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.109C>T
  hgvsp: ENSP00000373277.2:p.Pro37Ser
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5480
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4392
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3494
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5046
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2006
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3930
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3240
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1019
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro37Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/3-29476273-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476273
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476273
    reference: chr 3
allele count: 1
allele frequency: 8.251778258214646e-6
allele num: 121186
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.115A>C
  hgvsp: ENSP00000397926.1:p.Ser39Arg
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.115A>C
  hgvsp: ENSP00000373277.2:p.Ser39Arg
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.115A>C
  hgvsp: ENSP00000379828.3:p.Ser39Arg
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.614A>C
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.112A>C
  hgvsp: ENSP00000395592.1:p.Ser38Arg
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.115A>C
  hgvsp: ENSP00000273139.9:p.Ser39Arg
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.112A>C
  hgvsp: ENSP00000373276.2:p.Ser38Arg
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.115A>C
  hgvsp: ENSP00000400519.1:p.Ser39Arg
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.115A>C
  hgvsp: ENSP00000391934.1:p.Ser39Arg
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5473
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5040
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5181
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3240
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2592
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1610
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser39Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

3-29476277-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476277
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476277
    reference: chr 3
allele count: 8
allele frequency: 6.599571027883188e-5
allele num: 121220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.119C>T
  hgvsp: ENSP00000397926.1:p.Pro40Leu
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.119C>T
  hgvsp: ENSP00000379828.3:p.Pro40Leu
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.119C>T
  hgvsp: ENSP00000273139.9:p.Pro40Leu
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.119C>T
  hgvsp: ENSP00000391934.1:p.Pro40Leu
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.119C>T
  hgvsp: ENSP00000400519.1:p.Pro40Leu
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.116C>T
  hgvsp: ENSP00000373276.2:p.Pro39Leu
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.116C>T
  hgvsp: ENSP00000395592.1:p.Pro39Leu
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.618C>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.119C>T
  hgvsp: ENSP00000373277.2:p.Pro40Leu
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5184
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2004
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3469
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3928
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4598
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro40Leu
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

3-29476289-GCAGCAGCAACAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476289
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476277
    reference: chr 3
allele count: 11
allele frequency: 9.069920844327176e-5
allele num: 121280
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsp: ENSP00000373277.2:p.Asn51_Ser54del
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsp: ENSP00000400519.1:p.Asn51_Ser54del
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsp: ENSP00000373276.2:p.Asn50_Ser53del
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsp: ENSP00000379828.3:p.Asn51_Ser54del
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsp: ENSP00000395592.1:p.Asn50_Ser53del
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsp: ENSP00000391934.1:p.Asn51_Ser54del
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsp: ENSP00000273139.9:p.Asn51_Ser54del
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsp: ENSP00000397926.1:p.Asn51_Ser54del
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3239
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4367
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1154
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn51_Ser54del
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: GCAGCAGCAACAA
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

3-29476295-GCAACAACAGCAGCAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476295
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476280
    reference: chr 3
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsp: ENSP00000400519.1:p.Asn48_Asn52del
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsp: ENSP00000391934.1:p.Asn48_Asn52del
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsp: ENSP00000395592.1:p.Asn47_Asn51del
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsp: ENSP00000397926.1:p.Asn48_Asn52del
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsp: ENSP00000373276.2:p.Asn47_Asn51del
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsp: ENSP00000273139.9:p.Asn48_Asn52del
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsp: ENSP00000379828.3:p.Asn48_Asn52del
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsp: ENSP00000373277.2:p.Asn48_Asn52del
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5171
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4358
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3477
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4536
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5472
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2589
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1773
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44611
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Asn48_Asn52del
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: GCAACAACAGCAGCAA
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP

3-29476315-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476315
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476315
    reference: chr 3
allele count: 41
allele frequency: 3.37887953058298e-4
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.157A>T
  hgvsp: ENSP00000379828.3:p.Ser53Cys
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.157A>T
  hgvsp: ENSP00000373277.2:p.Ser53Cys
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.157A>T
  hgvsp: ENSP00000391934.1:p.Ser53Cys
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.157A>T
  hgvsp: ENSP00000273139.9:p.Ser53Cys
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.154A>T
  hgvsp: ENSP00000395592.1:p.Ser52Cys
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.157A>T
  hgvsp: ENSP00000400519.1:p.Ser53Cys
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.656A>T
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.154A>T
  hgvsp: ENSP00000373276.2:p.Ser52Cys
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.157A>T
  hgvsp: ENSP00000397926.1:p.Ser53Cys
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5170
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2001
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5045
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5041
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4538
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4356
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 5.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6576
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser53Cys
num of homozygotes: 1
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ

3-29476316-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476316
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476316
    reference: chr 3
allele count: 1
allele frequency: 8.241441263248117e-6
allele num: 121338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.155G>A
  hgvsp: ENSP00000373276.2:p.Ser52Asn
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.657G>A
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.158G>A
  hgvsp: ENSP00000373277.2:p.Ser53Asn
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.158G>A
  hgvsp: ENSP00000397926.1:p.Ser53Asn
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.158G>A
  hgvsp: ENSP00000391934.1:p.Ser53Asn
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.158G>A
  hgvsp: ENSP00000273139.9:p.Ser53Asn
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.158G>A
  hgvsp: ENSP00000379828.3:p.Ser53Asn
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.155G>A
  hgvsp: ENSP00000395592.1:p.Ser52Asn
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.158G>A
  hgvsp: ENSP00000400519.1:p.Ser53Asn
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3150
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5044
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4594
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4533
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2002
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser53Asn
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

3-29476318-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 29476318
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 29476318
    reference: chr 3
allele count: 7
allele frequency: 5.768533473975673e-5
allele num: 121348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000400519
  ensembl transcript: ENST00000456853
  gene symbol: RBMS3
  hgvsc: ENST00000456853.1:c.160A>G
  hgvsp: ENSP00000400519.1:p.Ser54Gly
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373276
  ensembl transcript: ENST00000383766
  gene symbol: RBMS3
  hgvsc: ENST00000383766.2:c.157A>G
  hgvsp: ENSP00000373276.2:p.Ser53Gly
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000391934
  ensembl transcript: ENST00000445033
  gene symbol: RBMS3
  hgvsc: ENST00000445033.1:c.160A>G
  hgvsp: ENSP00000391934.1:p.Ser54Gly
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000273139
  ensembl transcript: ENST00000273139
  gene symbol: RBMS3
  hgvsc: ENST00000273139.9:c.160A>G
  hgvsp: ENSP00000273139.9:p.Ser54Gly
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000144642
  ensembl transcript: ENST00000471426
  gene symbol: RBMS3
  hgvsc: ENST00000471426.1:n.659A>G
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000379828
  ensembl transcript: ENST00000396583
  gene symbol: RBMS3
  hgvsc: ENST00000396583.3:c.160A>G
  hgvsp: ENSP00000379828.3:p.Ser54Gly
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000397926
  ensembl transcript: ENST00000452462
  gene symbol: RBMS3
  hgvsc: ENST00000452462.1:c.160A>G
  hgvsp: ENSP00000397926.1:p.Ser54Gly
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000373277
  ensembl transcript: ENST00000383767
  gene symbol: RBMS3
  hgvsc: ENST00000383767.2:c.160A>G
  hgvsp: ENSP00000373277.2:p.Ser54Gly
  variant of: http://identifiers.org/hgnc/13427
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000144642
  ensembl protein: ENSP00000395592
  ensembl transcript: ENST00000434693
  gene symbol: RBMS3
  hgvsc: ENST00000434693.2:c.157A>G
  hgvsp: ENSP00000395592.1:p.Ser53Gly
  variant of: http://identifiers.org/hgnc/13427
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3925
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5043
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5042
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2587
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3487
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3238
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3488
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5474
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4534
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44616
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ser54Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 2.121212121212121e-2
allele num: 330
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.333333333333333e-2
allele num: 30
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.75e-2
allele num: 160
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.061e-1

DP
type: SiteQuality
SIO_000300: 4.3032e4

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

QD
type: SiteQuality
SIO_000300: 7.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

FS
type: SiteQuality
SIO_000300: 4.291e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

Other
type: Population
allele count: 1
allele frequency: 1.0e-1
allele num: 10
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.25e-2
allele num: 160
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.061e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.291e0

VQSLOD
type: SiteQuality
SIO_000300: 1.32e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.14e-1

QD
type: SiteQuality
SIO_000300: 7.0e0

DP
type: SiteQuality
SIO_000300: 4.3032e4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 104
num of homozygotes: 0

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

South Asian
type: Population
allele count: 6
allele frequency: 5.10204081632653e-3
allele num: 1176
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.3281e4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

QD
type: SiteQuality
SIO_000300: 1.069e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.16e-2

FS
type: SiteQuality
SIO_000300: 2.694e0

VQSLOD
type: SiteQuality
SIO_000300: 8.070000000000001e-1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 182
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
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FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.096e0

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.5e-1

DP
type: SiteQuality
SIO_000300: 4.3807e4

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.53e-2

VQSLOD
type: SiteQuality
SIO_000300: -8.093e-1

MQ
type: SiteQuality
SIO_000300: 5.685e1

QD
type: SiteQuality
SIO_000300: 1.039e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

Latino
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allele count: 3
allele frequency: 1.25e-1
allele num: 24
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 38
allele frequency: 1.225806451612903e-1
allele num: 310
num of homozygotes: 0

African
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allele count: 4
allele frequency: 6.060606060606061e-2
allele num: 66
num of homozygotes: 0

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

South Asian
type: Population
allele count: 122
allele frequency: 1.942675159235669e-1
allele num: 628
num of homozygotes: 1

FS
type: SiteQuality
SIO_000300: 8.86e-1

DP
type: SiteQuality
SIO_000300: 5.5451e4

QD
type: SiteQuality
SIO_000300: 3.19e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.45e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.059e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 40
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.592356687898089e-3
allele num: 628
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.0e-1
allele num: 10
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QD
type: SiteQuality
SIO_000300: 3.19e0

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.059e-1

FS
type: SiteQuality
SIO_000300: 8.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.45e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

DP
type: SiteQuality
SIO_000300: 5.5451e4

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 40
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

FS
type: SiteQuality
SIO_000300: 8.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.059e-1

QD
type: SiteQuality
SIO_000300: 3.19e0

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

DP
type: SiteQuality
SIO_000300: 5.5451e4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

African
type: Population
allele count: 3
allele frequency: 4.545454545454546e-2
allele num: 66
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 4.166666666666666e-2
allele num: 24
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 1.75e-1
allele num: 40
num of homozygotes: 0

South Asian
type: Population
allele count: 65
allele frequency: 1.035031847133758e-1
allele num: 628
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.059e-1

MQ
type: SiteQuality
SIO_000300: 5.936e1

QD
type: SiteQuality
SIO_000300: 3.19e0

MQRankSum
type: SiteQuality
SIO_000300: 3.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.54e-1

FS
type: SiteQuality
SIO_000300: 8.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

DP
type: SiteQuality
SIO_000300: 5.5451e4

VQSLOD
type: SiteQuality
SIO_000300: 3.45e0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 48
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Other
type: Population
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allele frequency: 0.0e0
allele num: 14
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 380
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.654e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.15e-1

DP
type: SiteQuality
SIO_000300: 5.4446e4

MQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

MQ
type: SiteQuality
SIO_000300: 5.913e1

QD
type: SiteQuality
SIO_000300: 6.86e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.61e-1

African
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allele count: 0
allele frequency: 0.0e0
allele num: 136
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1192
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

DP
type: SiteQuality
SIO_000300: 5.6788e4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.036e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.07e-2

QD
type: SiteQuality
SIO_000300: 1.496e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

MQ
type: SiteQuality
SIO_000300: 5.875e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -4.575e-1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 124
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1282
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 8.640552995391706e-4
allele num: 3472
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.08e0

MQRankSum
type: SiteQuality
SIO_000300: 7.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.8e-1

DP
type: SiteQuality
SIO_000300: 6.2974e4

MQ
type: SiteQuality
SIO_000300: 5.922e1

FS
type: SiteQuality
SIO_000300: 4.521e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.46e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1396
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.493765586034913e-4
allele num: 4010
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.02e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.151e0

DP
type: SiteQuality
SIO_000300: 6.8984e4

QD
type: SiteQuality
SIO_000300: 1.933e1

FS
type: SiteQuality
SIO_000300: 6.463e0

MQRankSum
type: SiteQuality
SIO_000300: 2.53e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1240
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 114
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 120
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.224e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.182e0

QD
type: SiteQuality
SIO_000300: 2.209e1

DP
type: SiteQuality
SIO_000300: 6.178e4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.05e-2

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

African
type: Population
allele count: 1
allele frequency: 1.76056338028169e-3
allele num: 568
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3792
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.913e1

QD
type: SiteQuality
SIO_000300: 1.002e1

MQRankSum
type: SiteQuality
SIO_000300: -4.3e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.321e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.84807e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.31e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.78e0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 184
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4036
num of homozygotes: 0

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
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VQSLOD
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DP
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ClippingRankSum
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InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 4.013e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e-1

QD
type: SiteQuality
SIO_000300: 1.537e1

Latino
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allele frequency: 5.319148936170213e-3
allele num: 188
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 586
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 4.948045522018803e-4
allele num: 4042
num of homozygotes: 0

South Asian
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allele frequency: 3.939075630252101e-4
allele num: 7616
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.65e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.08e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 2.551e0

VQSLOD
type: SiteQuality
SIO_000300: 2.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.77e0

DP
type: SiteQuality
SIO_000300: 1.96761e5

Other
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allele frequency: 0.0e0
allele num: 182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 580
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1586
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.938e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.75e-2

MQ
type: SiteQuality
SIO_000300: 5.894e1

MQRankSum
type: SiteQuality
SIO_000300: 4.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.92e-1

DP
type: SiteQuality
SIO_000300: 1.94827e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.62e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.44e0

QD
type: SiteQuality
SIO_000300: 1.136e1

GenotypeQuality
all individuals: 767
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variant carriers: 0

GenotypeQuality
all individuals: 2504
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3861
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8824
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1048
bin: 5.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10350
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6578
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8412
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.507068149621726e-5
allele num: 66354
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.931e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.099406e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.6e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.53e-1

QD
type: SiteQuality
SIO_000300: 9.619999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 8.92e-1

GenotypeQuality
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bin: 4.25e1
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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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9327
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2485
bin: 8.75e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20157
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

South Asian
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allele frequency: 0.0e0
allele num: 16422
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11436
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506977304921788e-5
allele num: 66358
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.78e0

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.100552e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.7e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.29e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.471e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.500000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e0

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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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8414
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.825261620832319e-4
allele num: 16436
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.011866755014758e-5
allele num: 66404
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

VQSLOD
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FS
type: SiteQuality
SIO_000300: 3.184e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.72e-1

DP
type: SiteQuality
SIO_000300: 2.115569e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e-1

QD
type: SiteQuality
SIO_000300: 1.581e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.977e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66420
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

Latino
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allele count: 7
allele frequency: 6.10394140216254e-4
allele num: 11468
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.92e-1

MQ
type: SiteQuality
SIO_000300: 5.903e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.111e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.41e-1

FS
type: SiteQuality
SIO_000300: 9.9e-1

QD
type: SiteQuality
SIO_000300: 1.21e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.64e-1

DP
type: SiteQuality
SIO_000300: 2.12398e6

VQSLOD
type: SiteQuality
SIO_000300: 5.86e-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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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8436
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504528631179851e-5
allele num: 66466
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16446
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 3.64e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.49e-1

FS
type: SiteQuality
SIO_000300: 4.312e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

DP
type: SiteQuality
SIO_000300: 2.131782e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.618e0

MQRankSum
type: SiteQuality
SIO_000300: 4.99e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.102e0

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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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.431019812811474e-4
allele num: 16454
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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QD
type: SiteQuality
SIO_000300: 1.014e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.21e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

DP
type: SiteQuality
SIO_000300: 2.133553e6

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.4e-3

FS
type: SiteQuality
SIO_000300: 8.099e0

VQSLOD
type: SiteQuality
SIO_000300: -8.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.12e-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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10370
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 902
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66498
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

South Asian
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.23e0

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: 1.09e-2

DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.208e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele num: 10382
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East Asian
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allele frequency: 1.178967224711153e-4
allele num: 8482
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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ClippingRankSum
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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
type: SiteQuality
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BaseQRankSum
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QD
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FS
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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Latino
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East Asian
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South Asian
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Other
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allele frequency: 0.0e0
allele num: 902
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European (Non-Finnish)
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allele frequency: 1.502403846153846e-5
allele num: 66560
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BaseQRankSum
type: SiteQuality
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QD
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FS
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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DP
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele frequency: 1.177301624676242e-4
allele num: 8494
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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Other
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South Asian
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European (Finnish)
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African
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allele frequency: 9.619084263178146e-5
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66560
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

InbreedingCoeff
type: SiteQuality
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DP
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VQSLOD
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MQ
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501862309263487e-5
allele num: 66584
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Other
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ReadPosRankSum
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MQRankSum
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DP
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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FS
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Non-Finnish)
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Latino
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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ClippingRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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MQRankSum
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DP
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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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African
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South Asian
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European (Non-Finnish)
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allele frequency: 6.006907944135756e-5
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European (Finnish)
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allele frequency: 0.0e0
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Other
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East Asian
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allele frequency: 0.0e0
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Latino
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MQRankSum
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SIO_000300: -2.3e-1

ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQ
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FS
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ReadPosRankSum
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QD
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InbreedingCoeff
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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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European (Non-Finnish)
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European (Finnish)
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South Asian
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African
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Other
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East Asian
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Latino
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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MQ
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DP
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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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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South Asian
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allele frequency: 0.0e0
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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Other
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QD
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MQ
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InbreedingCoeff
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DP
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BaseQRankSum
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FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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African
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Latino
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South Asian
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East Asian
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BaseQRankSum
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FS
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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MQ
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VQSLOD
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ClippingRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Other
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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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BaseQRankSum
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ClippingRankSum
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MQRankSum
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FS
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ReadPosRankSum
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QD
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VQSLOD
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MQ
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InbreedingCoeff
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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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European (Non-Finnish)
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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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Other
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East Asian
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FS
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QD
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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DP
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.965e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeQuality
all individuals: 15
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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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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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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bin: 7.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

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

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.76e-1

QD
type: SiteQuality
SIO_000300: 1.191e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.78e-2

FS
type: SiteQuality
SIO_000300: 2.496e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.39e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

MQRankSum
type: SiteQuality
SIO_000300: 2.84e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.59e-1

DP
type: SiteQuality
SIO_000300: 2.151029e6

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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
num of homozygotes: 0

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.93e-1

QD
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SIO_000300: 1.207e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.54e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.253e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.38e-1

DP
type: SiteQuality
SIO_000300: 2.150658e6

MQ
type: SiteQuality
SIO_000300: 5.805e1

FS
type: SiteQuality
SIO_000300: 3.123e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.606e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500915558490679e-5
allele num: 66626
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: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 7.184e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -9.15e-1

DP
type: SiteQuality
SIO_000300: 2.148441e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

QD
type: SiteQuality
SIO_000300: 8.050000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.149999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.583e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e0

MQ
type: SiteQuality
SIO_000300: 5.914e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66590
num of homozygotes: 0

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.16e0

VQSLOD
type: SiteQuality
SIO_000300: -6.63e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.47e-2

QD
type: SiteQuality
SIO_000300: 1.184e1

MQ
type: SiteQuality
SIO_000300: 5.911e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.8e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.144662e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

GenotypeQuality
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variant carriers: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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: 1
allele frequency: 1.501636784094663e-5
allele num: 66594
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.143924e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.32e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.3e-2

FS
type: SiteQuality
SIO_000300: 6.315e0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.28e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.541e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.82e-1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

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

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.00336376741951e-5
allele num: 66592
num of homozygotes: 0

DP
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.22e-2

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.975e1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.69e-1

MQRankSum
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BaseQRankSum
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SIO_000300: -3.997e0

QD
type: SiteQuality
SIO_000300: 1.079e1

GenotypeQuality
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bin: 4.25e1
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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bin: 9.75e1
variant carriers: 5

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

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

Latino
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allele frequency: 4.344803614876608e-4
allele num: 11508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
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South Asian
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allele num: 16434
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.05e-2

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.577e1

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 3.593e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.97e-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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bin: 6.75e1
variant carriers: 0

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

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

Other
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allele num: 904
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
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allele frequency: 9.615384615384615e-5
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.697e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
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VQSLOD
type: SiteQuality
SIO_000300: 1.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.87e0

GenotypeQuality
all individuals: 20255
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3928
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502448991856726e-5
allele num: 66558
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.76e-1

QD
type: SiteQuality
SIO_000300: 1.185e1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.003e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.84e-2

MQ
type: SiteQuality
SIO_000300: 5.959e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.684e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e0

DP
type: SiteQuality
SIO_000300: 2.131504e6

GenotypeQuality
all individuals: 335
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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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bin: 9.75e1
variant carriers: 9

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3925
bin: 9.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.058823529411765e-3
allele num: 8500
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.957e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.0e-1

DP
type: SiteQuality
SIO_000300: 2.122672e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.31e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.08e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.95e0

QD
type: SiteQuality
SIO_000300: 1.692e1

GenotypeQuality
all individuals: 443
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11038
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 517
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 3.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.091617933723197e-5
allele num: 16416
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: 11494
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: 0
allele frequency: 0.0e0
allele num: 66522
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -7.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

DP
type: SiteQuality
SIO_000300: 2.119279e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.48e0

QD
type: SiteQuality
SIO_000300: 1.562e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

MQ
type: SiteQuality
SIO_000300: 5.982e1

GenotypeQuality
all individuals: 11038
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3926
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variant carriers: 0

GenotypeQuality
all individuals: 70
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 20
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GenotypeQuality
all individuals: 497
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3326
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 840
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4909
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variant carriers: 0

GenotypeQuality
all individuals: 2559
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4597
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variant carriers: 0

GenotypeQuality
all individuals: 20254
bin: 9.75e1
variant carriers: 13

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

African
type: Population
allele count: 13
allele frequency: 1.249519415609381e-3
allele num: 10404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66522
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.982e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.48e0

MQRankSum
type: SiteQuality
SIO_000300: -7.77e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.23e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.15e-1

QD
type: SiteQuality
SIO_000300: 1.562e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

DP
type: SiteQuality
SIO_000300: 2.119279e6

GenotypeQuality
all individuals: 155
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 339
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variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 28
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GenotypeQuality
all individuals: 650
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variant carriers: 0

GenotypeQuality
all individuals: 533
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 44818
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 98
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variant carriers: 0

GenotypeQuality
all individuals: 2003
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variant carriers: 0

GenotypeQuality
all individuals: 1529
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1222
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64574
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.754194303550527e-5
allele num: 10252
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
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: 0
allele frequency: 0.0e0
allele num: 11222
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.48e-1

MQ
type: SiteQuality
SIO_000300: 5.92e1

QD
type: SiteQuality
SIO_000300: 1.607e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-3

DP
type: SiteQuality
SIO_000300: 3.581917e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.24e-1

FS
type: SiteQuality
SIO_000300: 6.868e0

MQRankSum
type: SiteQuality
SIO_000300: -9.419999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

GenotypeQuality
all individuals: 643
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 880
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 809
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variant carriers: 0

GenotypeQuality
all individuals: 611
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2059
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44816
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1725
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1120
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variant carriers: 0

GenotypeQuality
all individuals: 441
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1575
bin: 6.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11204
num of homozygotes: 0

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

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

African
type: Population
allele count: 3
allele frequency: 2.927971891469842e-4
allele num: 10246
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.752e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.26e0

DP
type: SiteQuality
SIO_000300: 3.582467e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.33e1

MQ
type: SiteQuality
SIO_000300: 5.886e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.74e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

GenotypeQuality
all individuals: 1997
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 874
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
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variant carriers: 0

GenotypeQuality
all individuals: 2207
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variant carriers: 0

GenotypeQuality
all individuals: 567
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GenotypeQuality
all individuals: 42
bin: 5.25e1
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GenotypeQuality
all individuals: 1118
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GenotypeQuality
all individuals: 116
bin: 4.75e1
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GenotypeQuality
all individuals: 1462
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1598
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 44867
bin: 9.75e1
variant carriers: 795

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.098661378284581e-5
allele num: 64544
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: 20
allele frequency: 1.743983257760725e-3
allele num: 11468
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8562
num of homozygotes: 0

African
type: Population
allele count: 802
allele frequency: 7.822863831447523e-2
allele num: 10252
num of homozygotes: 32

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11212
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.64963503649635e-3
allele num: 822
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.16e0

DP
type: SiteQuality
SIO_000300: 3.584489e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.363e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

MQRankSum
type: SiteQuality
SIO_000300: 2.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.39e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.97e-1

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

GenotypeQuality
all individuals: 158
bin: 2.5e0
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GenotypeQuality
all individuals: 1643
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 901
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
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GenotypeQuality
all individuals: 2032
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1143
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2251
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44650
bin: 9.75e1
variant carriers: 63

East Asian
type: Population
allele count: 62
allele frequency: 7.234539089848308e-3
allele num: 8570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11470
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.548802775454574e-5
allele num: 64566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11248
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.142e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.956e1

VQSLOD
type: SiteQuality
SIO_000300: 3.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.18e-1

FS
type: SiteQuality
SIO_000300: 1.75e0

QD
type: SiteQuality
SIO_000300: 1.212e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

DP
type: SiteQuality
SIO_000300: 3.545625e6

GenotypeQuality
all individuals: 1754
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2031
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.25e1
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GenotypeQuality
all individuals: 44650
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 332
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2691
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1493
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11472
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.547125440930751e-5
allele num: 64636
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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MQRankSum
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BaseQRankSum
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SIO_000300: 1.21e0

VQSLOD
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QD
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MQ
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ClippingRankSum
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SIO_000300: -1.57e0

InbreedingCoeff
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SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 3.853e0

DP
type: SiteQuality
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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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Other
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allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.153467478924374e-5
allele num: 65004
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
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DP
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
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MQ
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VQSLOD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.537468097536976e-5
allele num: 65042
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

ClippingRankSum
type: SiteQuality
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QD
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MQRankSum
type: SiteQuality
SIO_000300: 7.94e-1

InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.08e-1

VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: -4.51e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

DP
type: SiteQuality
SIO_000300: 3.564956e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.99e-1

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

East Asian
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allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 13348
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65308
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.686e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.578316e6

MQ
type: SiteQuality
SIO_000300: 5.949e1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.15e-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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variant carriers: 15

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65484
num of homozygotes: 0

African
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allele frequency: 1.25676720804331e-3
allele num: 10344
num of homozygotes: 0

Latino
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allele count: 2
allele frequency: 1.735207357279195e-4
allele num: 11526
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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8616
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: 882
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MQ
type: SiteQuality
SIO_000300: 5.925e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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DP
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.42e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65522
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Other
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allele num: 884
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East Asian
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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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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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DP
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VQSLOD
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QD
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MQRankSum
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FS
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 1.732201628269531e-4
allele num: 11546
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African
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South Asian
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East Asian
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ClippingRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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DP
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VQSLOD
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MQRankSum
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ReadPosRankSum
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QD
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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East Asian
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European (Finnish)
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South Asian
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Other
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African
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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MQ
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BaseQRankSum
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MQRankSum
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DP
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FS
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Non-Finnish)
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European (Finnish)
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African
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East Asian
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Other
type: Population
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South Asian
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DP
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FS
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ReadPosRankSum
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QD
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BaseQRankSum
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MQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

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

African
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allele frequency: 0.0e0
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Other
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.506024096385542e-5
allele num: 66400
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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MQRankSum
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VQSLOD
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BaseQRankSum
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MQ
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ClippingRankSum
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QD
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FS
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InbreedingCoeff
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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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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66424
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African
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allele count: 2
allele frequency: 1.92270717169775e-4
allele num: 10402
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Latino
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allele frequency: 0.0e0
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BaseQRankSum
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VQSLOD
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MQRankSum
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FS
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MQ
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InbreedingCoeff
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ClippingRankSum
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QD
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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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
allele num: 10400
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Latino
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allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
allele num: 900
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.010416039496658e-5
allele num: 66436
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66556
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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 count: 2
allele frequency: 1.221001221001221e-4
allele num: 16380
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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FS
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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QD
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MQ
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DP
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ClippingRankSum
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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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Other
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European (Finnish)
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African
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European (Non-Finnish)
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East Asian
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Latino
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South Asian
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VQSLOD
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QD
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InbreedingCoeff
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MQRankSum
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FS
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MQ
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ClippingRankSum
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BaseQRankSum
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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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East Asian
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African
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European (Non-Finnish)
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Latino
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Other
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European (Finnish)
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South Asian
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ReadPosRankSum
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VQSLOD
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DP
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FS
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MQ
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InbreedingCoeff
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MQRankSum
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QD
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BaseQRankSum
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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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East Asian
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Other
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African
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European (Finnish)
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Latino
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South Asian
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European (Non-Finnish)
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MQ
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FS
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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MQRankSum
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DP
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Non-Finnish)
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European (Finnish)
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Other
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African
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Latino
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InbreedingCoeff
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QD
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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MQRankSum
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FS
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ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 5.46e1

DP
type: SiteQuality
SIO_000300: 3.629976e6

GenotypeQuality
all individuals: 1809
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1012
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1779
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2029
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1155
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1602
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44632
bin: 9.75e1
variant carriers: 40

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

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

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

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

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

South Asian
type: Population
allele count: 33
allele frequency: 1.999030772958565e-3
allele num: 16508
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.049758555532228e-4
allele num: 66682
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.341e1

VQSLOD
type: SiteQuality
SIO_000300: 5.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.29e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.96e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.57e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.631391e6

MQRankSum
type: SiteQuality
SIO_000300: 2.73e-1

MQ
type: SiteQuality
SIO_000300: 5.96e1

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

GenotypeQuality
all individuals: 44616
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1810
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1156
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1015
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1599
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2029
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6590
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1776
bin: 8.25e1
variant carriers: 0

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66682
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.876e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.394e0

QD
type: SiteQuality
SIO_000300: 1.3e1

DP
type: SiteQuality
SIO_000300: 3.630663e6

MQRankSum
type: SiteQuality
SIO_000300: -9.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.336e0

VQSLOD
type: SiteQuality
SIO_000300: -1.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.109e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.52e0

GenotypeQuality
all individuals: 1814
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1599
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6591
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1015
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1778
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2030
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 7
allele frequency: 6.045949214026602e-4
allele num: 11578
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.44e0

QD
type: SiteQuality
SIO_000300: 1.446e1

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-3

DP
type: SiteQuality
SIO_000300: 3.630623e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4