15-74726255-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74726255
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74726255
    reference: chr 15
allele count: 1
allele frequency: 1.470588235294118e-2
allele num: 68
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138623
  ensembl protein: ENSP00000438966
  ensembl transcript: ENST00000543145
  gene symbol: SEMA7A
  hgvsc: ENST00000543145.2:c.5C>T
  hgvsp: ENSP00000438966.2:p.Thr2Met
  variant of: http://identifiers.org/hgnc/10741
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138623
  ensembl protein: ENSP00000261918
  ensembl transcript: ENST00000261918
  gene symbol: SEMA7A
  hgvsc: ENST00000261918.4:c.5C>T
  hgvsp: ENSP00000261918.4:p.Thr2Met
  variant of: http://identifiers.org/hgnc/10741
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23324
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  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
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22244
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1502
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr2Met
num of homozygotes: 0
population: East Asian
  type: Population
  allele count: 1
  allele frequency: 1.666666666666667e-1
  allele num: 6
  num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

15-74726271-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74726271
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74726271
    reference: chr 15
allele count: 2
allele frequency: 2.631578947368421e-2
allele num: 76
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138623
  ensembl protein: ENSP00000438966
  ensembl transcript: ENST00000543145
  gene symbol: SEMA7A
  hgvsc: ENST00000543145.2:c.-12C>T
  variant of: http://identifiers.org/hgnc/10741
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138623
  ensembl protein: ENSP00000261918
  ensembl transcript: ENST00000261918
  gene symbol: SEMA7A
  hgvsc: ENST00000261918.4:c.-12C>T
  variant of: http://identifiers.org/hgnc/10741
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23965
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1368
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22680
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
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genotype quality: GenotypeQuality
  all individuals: 1425
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 0
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genotype quality: GenotypeQuality
  all individuals: 0
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 1
population: East Asian
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2
  num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD

15-74726283-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74726283
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74726283
    reference: chr 15
allele count: 1
allele frequency: 1.5625e-2
allele num: 64
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138623
  ensembl protein: ENSP00000438966
  ensembl transcript: ENST00000543145
  gene symbol: SEMA7A
  hgvsc: ENST00000543145.2:c.-24C>T
  variant of: http://identifiers.org/hgnc/10741
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138623
  ensembl protein: ENSP00000261918
  ensembl transcript: ENST00000261918
  gene symbol: SEMA7A
  hgvsc: ENST00000261918.4:c.-24C>T
  variant of: http://identifiers.org/hgnc/10741
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23758
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2042
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 4.25e1
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genotype quality: GenotypeQuality
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  bin: 5.25e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
  all individuals: 1
  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 205
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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: 0
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2
  num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

15-74726290-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74726290
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74726290
    reference: chr 15
allele count: 0
allele frequency: 0.0e0
allele num: 64
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138623
  ensembl protein: ENSP00000438966
  ensembl transcript: ENST00000543145
  gene symbol: SEMA7A
  hgvsc: ENST00000543145.2:c.-31T>A
  variant of: http://identifiers.org/hgnc/10741
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000138623
  ensembl protein: ENSP00000261918
  ensembl transcript: ENST00000261918
  gene symbol: SEMA7A
  hgvsc: ENST00000261918.4:c.-31T>A
  variant of: http://identifiers.org/hgnc/10741
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23623
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  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
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genotype depth: GenotypeDepth
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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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  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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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 2417
  bin: 2.5e0
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genotype quality: GenotypeQuality
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  variant carriers: 1
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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  variant carriers: 3
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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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: 273
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
  type: Population
  allele count: 0
  allele frequency: 0.0e0
  allele num: 2
  num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

15-74738397-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738397
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738397
    reference: chr 15
allele count: 4
allele frequency: 3.361118580263512e-5
allele num: 119008
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.*34C>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.*34C>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.*34C>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.*34C>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.*34C>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.*34C>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.*34C>G
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9332
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10836
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3964
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4745
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4515
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12346
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS

http://identifiers.org/exac.variant/15-74738398-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738398
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738398
    reference: chr 15
allele count: 11
allele frequency: 9.246805648957633e-5
allele num: 118960
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.*33G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.*33G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.*33G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.*33G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.*33G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.*33G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.*33G>T
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4872
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2077
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10851
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7631
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4747
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2856
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4511
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5880
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1369
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3962
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 631
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD

15-74738400-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738400
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738400
    reference: chr 15
allele count: 4
allele frequency: 3.358127508101483e-5
allele num: 119114
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.*31T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.*31T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.*31T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.*31T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.*31T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.*31T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.*31T>C
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9654
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7628
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5106
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2143
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3967
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1340
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

15-74738435-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738435
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738435
    reference: chr 15
allele count: 1
allele frequency: 8.304406317992327e-6
allele num: 120418
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1139C>A
  hgvsp: ENSP00000457708.1:p.Pro380Gln
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1139C>A
  hgvsp: ENSP00000354883.4:p.Pro380Gln
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1139C>A
  hgvsp: ENSP00000454828.1:p.Pro380Gln
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.544C>A
  hgvsp: ENSP00000456807.1:p.Pro182Gln
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.341C>A
  hgvsp: ENSP00000456662.1:p.Pro114Gln
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1139C>A
  hgvsp: ENSP00000378518.2:p.Pro380Gln
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1139C>A
  hgvsp: ENSP00000457703.1:p.Pro380Gln
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6939
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7623
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10963
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2378
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3964
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro380Gln
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum

15-74738439-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738439
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738439
    reference: chr 15
allele count: 3
allele frequency: 2.488841693076042e-5
allele num: 120538
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1135G>A
  hgvsp: ENSP00000457708.1:p.Ala379Thr
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1135G>A
  hgvsp: ENSP00000457703.1:p.Ala379Thr
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1135G>A
  hgvsp: ENSP00000454828.1:p.Ala379Thr
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1135G>A
  hgvsp: ENSP00000354883.4:p.Ala379Thr
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.337G>A
  hgvsp: ENSP00000456662.1:p.Ala113Thr
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.540G>A
  hgvsp: ENSP00000456807.1:p.Ala181Thr
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1135G>A
  hgvsp: ENSP00000378518.2:p.Ala379Thr
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9339
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7624
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5349
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3964
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18982
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2378
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala379Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ

15-74738442-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738442
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738442
    reference: chr 15
allele count: 1
allele frequency: 8.290774026663129e-6
allele num: 120616
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1132G>A
  hgvsp: ENSP00000354883.4:p.Gly378Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1132G>A
  hgvsp: ENSP00000454828.1:p.Gly378Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.334G>A
  hgvsp: ENSP00000456662.1:p.Gly112Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1132G>A
  hgvsp: ENSP00000378518.2:p.Gly378Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.537G>A
  hgvsp: ENSP00000456807.1:p.Gly180Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1132G>A
  hgvsp: ENSP00000457703.1:p.Gly378Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1132G>A
  hgvsp: ENSP00000457708.1:p.Gly378Arg
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10884
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4527
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6191
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3964
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly378Arg
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

15-74738445-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738445
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738445
    reference: chr 15
allele count: 1
allele frequency: 8.288162845823595e-6
allele num: 120654
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1129G>A
  hgvsp: ENSP00000354883.4:p.Gly377Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1129G>A
  hgvsp: ENSP00000454828.1:p.Gly377Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1129G>A
  hgvsp: ENSP00000457703.1:p.Gly377Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1129G>A
  hgvsp: ENSP00000378518.2:p.Gly377Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.534G>A
  hgvsp: ENSP00000456807.1:p.Gly179Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1129G>A
  hgvsp: ENSP00000457708.1:p.Gly377Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.331G>A
  hgvsp: ENSP00000456662.1:p.Gly111Arg
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10995
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7053
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6198
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3964
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly377Arg
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

15-74738455-G-GAGCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738455
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738459
    reference: chr 15
allele count: 1
allele frequency: 8.277323444690924e-6
allele num: 120812
alternate allele: GAGCT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1115_1118dupAGCT
  hgvsp: ENSP00000454828.1:p.Ile374AlafsTer31
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.520_523dupAGCT
  hgvsp: ENSP00000456807.1:p.Ile176AlafsTer31
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1115_1118dupAGCT
  hgvsp: ENSP00000457703.1:p.Ile374AlafsTer31
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1115_1118dupAGCT
  hgvsp: ENSP00000354883.4:p.Ile374AlafsTer31
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1115_1118dupAGCT
  hgvsp: ENSP00000378518.2:p.Ile374AlafsTer31
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.317_320dupAGCT
  hgvsp: ENSP00000456662.1:p.Ile108AlafsTer31
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1115_1118dupAGCT
  hgvsp: ENSP00000457708.1:p.Ile374AlafsTer31
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7620
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11024
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11011
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2380
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2925
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4769
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile374AlafsTer31
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP

15-74738464-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738464
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738464
    reference: chr 15
allele count: 1
allele frequency: 8.272256506129742e-6
allele num: 120886
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.312C>T
  hgvsp: ENST00000565494.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1110C>T
  hgvsp: ENST00000395081.2:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1110C>T
  hgvsp: ENST00000567435.1:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.515C>T
  hgvsp: ENST00000566365.1:c.515C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1110C>T
  hgvsp: ENST00000361351.4:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1110C>T
  hgvsp: ENST00000564488.1:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1110C>T
  hgvsp: ENST00000565335.1:c.1110C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2922
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18975
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4769
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala370Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

15-74738473-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738473
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738473
    reference: chr 15
allele count: 1
allele frequency: 8.269246671628215e-6
allele num: 120930
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.303C>G
  hgvsp: ENSP00000456662.1:p.Ile101Met
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1101C>G
  hgvsp: ENSP00000457703.1:p.Ile367Met
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1101C>G
  hgvsp: ENSP00000454828.1:p.Ile367Met
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1101C>G
  hgvsp: ENSP00000354883.4:p.Ile367Met
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1101C>G
  hgvsp: ENSP00000378518.2:p.Ile367Met
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1101C>G
  hgvsp: ENSP00000457708.1:p.Ile367Met
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.506C>G
  hgvsp: ENSP00000456807.1:p.Ile169Met
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16240
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2380
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile367Met
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

15-74738483-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738483
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738483
    reference: chr 15
allele count: 1
allele frequency: 8.267742575567167e-6
allele num: 120952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1091G>A
  hgvsp: ENSP00000457708.1:p.Gly364Asp
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1091G>A
  hgvsp: ENSP00000454828.1:p.Gly364Asp
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.496G>A
  hgvsp: ENSP00000456807.1:p.Gly166Asp
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1091G>A
  hgvsp: ENSP00000378518.2:p.Gly364Asp
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.293G>A
  hgvsp: ENSP00000456662.1:p.Gly98Asp
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1091G>A
  hgvsp: ENSP00000354883.4:p.Gly364Asp
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1091G>A
  hgvsp: ENSP00000457703.1:p.Gly364Asp
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2930
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2378
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly364Asp
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

15-74738484-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738484
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738484
    reference: chr 15
allele count: 1
allele frequency: 8.269109913008963e-6
allele num: 120932
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1090G>A
  hgvsp: ENSP00000457708.1:p.Gly364Ser
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.495G>A
  hgvsp: ENSP00000456807.1:p.Gly166Ser
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1090G>A
  hgvsp: ENSP00000457703.1:p.Gly364Ser
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1090G>A
  hgvsp: ENSP00000378518.2:p.Gly364Ser
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.292G>A
  hgvsp: ENSP00000456662.1:p.Gly98Ser
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1090G>A
  hgvsp: ENSP00000354883.4:p.Gly364Ser
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1090G>A
  hgvsp: ENSP00000454828.1:p.Gly364Ser
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4772
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16073
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2932
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gly364Ser
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

15-74738485-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738485
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738485
    reference: chr 15
allele count: 6
allele frequency: 4.960153434079561e-5
allele num: 120964
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1089C>T
  hgvsp: ENST00000567435.1:c.1089C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1089C>T
  hgvsp: ENST00000395081.2:c.1089C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1089C>T
  hgvsp: ENST00000361351.4:c.1089C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1089C>T
  hgvsp: ENST00000564488.1:c.1089C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1089C>T
  hgvsp: ENST00000565335.1:c.1089C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.291C>T
  hgvsp: ENST00000565494.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.494C>T
  hgvsp: ENST00000566365.1:c.494C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3397
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9354
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16201
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4776
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr363Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

15-74738498-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738498
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738497
    reference: chr 15
allele count: 1
allele frequency: 8.263370132874991e-6
allele num: 121016
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1075delG
  hgvsp: ENSP00000454828.1:p.Ala359ProfsTer?
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1075delG
  hgvsp: ENSP00000354883.4:p.Ala359ProfsTer?
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.480delG
  hgvsp: ENSP00000456807.1:p.Ala161ProfsTer?
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1075delG
  hgvsp: ENSP00000457708.1:p.Ala359ProfsTer?
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1075delG
  hgvsp: ENSP00000457703.1:p.Ala359ProfsTer?
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.277delG
  hgvsp: ENSP00000456662.1:p.Ala93ProfsTer?
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1075delG
  hgvsp: ENSP00000378518.2:p.Ala359ProfsTer?
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11198
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18968
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6215
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16232
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala359ProfsTer?
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: GC
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum

15-74738500-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738500
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738500
    reference: chr 15
allele count: 2
allele frequency: 1.652701340340787e-5
allele num: 121014
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1074G>A
  hgvsp: ENST00000567435.1:c.1074G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.479G>A
  hgvsp: ENST00000566365.1:c.479G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1074G>A
  hgvsp: ENST00000361351.4:c.1074G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1074G>A
  hgvsp: ENST00000565335.1:c.1074G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1074G>A
  hgvsp: ENST00000564488.1:c.1074G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1074G>A
  hgvsp: ENST00000395081.2:c.1074G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.276G>A
  hgvsp: ENST00000565494.1:c.276G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4524
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2930
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg358Arg
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum

15-74738502-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738502
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738502
    reference: chr 15
allele count: 2
allele frequency: 1.652592090694254e-5
allele num: 121022
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1072C>T
  hgvsp: ENSP00000457708.1:p.Arg358Trp
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1072C>T
  hgvsp: ENSP00000457703.1:p.Arg358Trp
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.477C>T
  hgvsp: ENSP00000456807.1:p.Arg160Trp
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1072C>T
  hgvsp: ENSP00000454828.1:p.Arg358Trp
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1072C>T
  hgvsp: ENSP00000378518.2:p.Arg358Trp
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.274C>T
  hgvsp: ENSP00000456662.1:p.Arg92Trp
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1072C>T
  hgvsp: ENSP00000354883.4:p.Arg358Trp
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11050
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4526
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2376
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2926
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg358Trp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

15-74738516-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738516
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738516
    reference: chr 15
allele count: 1
allele frequency: 8.258865892535638e-6
allele num: 121082
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.260A>G
  hgvsp: ENSP00000456662.1:p.Asp87Gly
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1058A>G
  hgvsp: ENSP00000457703.1:p.Asp353Gly
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1058A>G
  hgvsp: ENSP00000454828.1:p.Asp353Gly
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.463A>G
  hgvsp: ENSP00000456807.1:p.Asp155Gly
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1058A>G
  hgvsp: ENSP00000457708.1:p.Asp353Gly
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1058A>G
  hgvsp: ENSP00000354883.4:p.Asp353Gly
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1058A>G
  hgvsp: ENSP00000378518.2:p.Asp353Gly
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9352
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6221
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2923
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4783
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp353Gly
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

15-74738518-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738518
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738518
    reference: chr 15
allele count: 8
allele frequency: 6.607201850016519e-5
allele num: 121080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1056C>T
  hgvsp: ENST00000565335.1:c.1056C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.258C>T
  hgvsp: ENST00000565494.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1056C>T
  hgvsp: ENST00000361351.4:c.1056C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.461C>T
  hgvsp: ENST00000566365.1:c.461C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1056C>T
  hgvsp: ENST00000395081.2:c.1056C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1056C>T
  hgvsp: ENST00000564488.1:c.1056C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1056C>T
  hgvsp: ENST00000567435.1:c.1056C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6964
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11052
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9351
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4528
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4781
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16291
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp352Asp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

15-74738519-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738519
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738519
    reference: chr 15
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1055A>G
  hgvsp: ENSP00000354883.4:p.Asp352Gly
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1055A>G
  hgvsp: ENSP00000457708.1:p.Asp352Gly
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1055A>G
  hgvsp: ENSP00000454828.1:p.Asp352Gly
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1055A>G
  hgvsp: ENSP00000378518.2:p.Asp352Gly
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.257A>G
  hgvsp: ENSP00000456662.1:p.Asp86Gly
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1055A>G
  hgvsp: ENSP00000457703.1:p.Asp352Gly
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.460A>G
  hgvsp: ENSP00000456807.1:p.Asp154Gly
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2137
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6967
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3391
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2375
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4782
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asp352Gly
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-74738537-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738537
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738537
    reference: chr 15
allele count: 3
allele frequency: 2.477741621103751e-5
allele num: 121078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1037G>T
  hgvsp: ENSP00000457708.1:p.Arg346Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1037G>T
  hgvsp: ENSP00000454828.1:p.Arg346Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1037G>T
  hgvsp: ENSP00000354883.4:p.Arg346Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1037G>T
  hgvsp: ENSP00000378518.2:p.Arg346Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.239G>T
  hgvsp: ENSP00000456662.1:p.Arg80Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.442G>T
  hgvsp: ENSP00000456807.1:p.Arg148Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1037G>T
  hgvsp: ENSP00000457703.1:p.Arg346Leu
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11031
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18960
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg346Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

15-74738538-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738538
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738538
    reference: chr 15
allele count: 3
allele frequency: 2.478028150399789e-5
allele num: 121064
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1036C>T
  hgvsp: ENSP00000378518.2:p.Arg346Cys
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.441C>T
  hgvsp: ENSP00000456807.1:p.Arg148Cys
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.238C>T
  hgvsp: ENSP00000456662.1:p.Arg80Cys
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1036C>T
  hgvsp: ENSP00000354883.4:p.Arg346Cys
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1036C>T
  hgvsp: ENSP00000454828.1:p.Arg346Cys
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1036C>T
  hgvsp: ENSP00000457708.1:p.Arg346Cys
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1036C>T
  hgvsp: ENSP00000457703.1:p.Arg346Cys
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3393
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2136
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2915
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15796
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 496
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg346Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

15-74738548-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738548
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738548
    reference: chr 15
allele count: 2
allele frequency: 1.653849334325643e-5
allele num: 120930
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.431G>A
  hgvsp: ENST00000566365.1:c.431G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1026G>A
  hgvsp: ENST00000567435.1:c.1026G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1026G>A
  hgvsp: ENST00000564488.1:c.1026G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1026G>A
  hgvsp: ENST00000361351.4:c.1026G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.228G>A
  hgvsp: ENST00000565494.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1026G>A
  hgvsp: ENST00000395081.2:c.1026G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1026G>A
  hgvsp: ENST00000565335.1:c.1026G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9225
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15025
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 300
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2831
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu342Leu
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

15-74738552-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738552
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738552
    reference: chr 15
allele count: 2
allele frequency: 1.661709234118214e-5
allele num: 120358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1022A>C
  hgvsp: ENSP00000454828.1:p.Gln341Pro
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.224A>C
  hgvsp: ENSP00000456662.1:p.Gln75Pro
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1022A>C
  hgvsp: ENSP00000378518.2:p.Gln341Pro
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1022A>C
  hgvsp: ENSP00000457708.1:p.Gln341Pro
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1022A>C
  hgvsp: ENSP00000457703.1:p.Gln341Pro
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.427A>C
  hgvsp: ENSP00000456807.1:p.Gln143Pro
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1022A>C
  hgvsp: ENSP00000354883.4:p.Gln341Pro
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3333
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6817
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10973
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4482
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5633
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18945
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2781
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gln341Pro
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

15-74738555-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738555
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738555
    reference: chr 15
allele count: 1
allele frequency: 8.268562923763849e-6
allele num: 120940
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1019C>T
  hgvsp: ENSP00000457703.1:p.Pro340Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.424C>T
  hgvsp: ENSP00000456807.1:p.Pro142Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1019C>T
  hgvsp: ENSP00000457708.1:p.Pro340Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1019C>T
  hgvsp: ENSP00000454828.1:p.Pro340Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.221C>T
  hgvsp: ENSP00000456662.1:p.Pro74Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1019C>T
  hgvsp: ENSP00000378518.2:p.Pro340Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1019C>T
  hgvsp: ENSP00000354883.4:p.Pro340Leu
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10669
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9385
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5889
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4675
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro340Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

15-74738555-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738555
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738555
    reference: chr 15
allele count: 1
allele frequency: 8.268562923763849e-6
allele num: 120940
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.221C>A
  hgvsp: ENSP00000456662.1:p.Pro74His
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1019C>A
  hgvsp: ENSP00000354883.4:p.Pro340His
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1019C>A
  hgvsp: ENSP00000454828.1:p.Pro340His
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1019C>A
  hgvsp: ENSP00000457708.1:p.Pro340His
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.424C>A
  hgvsp: ENSP00000456807.1:p.Pro142His
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1019C>A
  hgvsp: ENSP00000457703.1:p.Pro340His
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1019C>A
  hgvsp: ENSP00000378518.2:p.Pro340His
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10669
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 780
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3456
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9385
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5400
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1302
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14553
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2421
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4884
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2912
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 247
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro340His
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

15-74738556-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738556
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738556
    reference: chr 15
allele count: 65
allele frequency: 5.674477075112616e-4
allele num: 114548
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1018C>G
  hgvsp: ENSP00000457703.1:p.Pro340Ala
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1018C>G
  hgvsp: ENSP00000457708.1:p.Pro340Ala
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1018C>G
  hgvsp: ENSP00000354883.4:p.Pro340Ala
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1018C>G
  hgvsp: ENSP00000378518.2:p.Pro340Ala
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.423C>G
  hgvsp: ENSP00000456807.1:p.Pro142Ala
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.220C>G
  hgvsp: ENSP00000456662.1:p.Pro74Ala
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1018C>G
  hgvsp: ENSP00000454828.1:p.Pro340Ala
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7506
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6533
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5237
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10703
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9245
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 10951
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.75e1
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 5384
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 3.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2303
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 18578
  bin: 9.75e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4356
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 1.25e1
  variant carriers: 1
hgvs: p.Pro340Ala
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

15-74738571-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738571
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738571
    reference: chr 15
allele count: 2
allele frequency: 1.654697686732634e-5
allele num: 120868
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1006-3C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.411-3C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1006-3C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1006-3C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1006-3C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.208-3C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1006-3C>T
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7525
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5641
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 2.75e1
  variant carriers: 0
hgvs: c.1006-3C>T
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum

15-74738580-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738580
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738580
    reference: chr 15
allele count: 1
allele frequency: 8.285553309249991e-6
allele num: 120692
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1006-12A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.208-12A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1006-12A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1006-12A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.411-12A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1006-12A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1006-12A>G
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7525
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5269
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10777
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10975
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14014
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/15-74738581-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738581
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738581
    reference: chr 15
allele count: 9
allele frequency: 7.459717525363039e-5
allele num: 120648
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.411-13T>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1006-13T>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1006-13T>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1006-13T>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1006-13T>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.208-13T>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1006-13T>G
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10978
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5270
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9239
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3970
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20817
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5554
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4516
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

15-74738582-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738582
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738582
    reference: chr 15
allele count: 2
allele frequency: 1.657769967839263e-5
allele num: 120644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1006-14C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.208-14C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1006-14C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1006-14C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1006-14C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.411-14C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1006-14C>T
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10736
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7525
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 894
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2384
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4517
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3971
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/15-74738590-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738590
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738590
    reference: chr 15
allele count: 3
allele frequency: 2.48970920196521e-5
allele num: 120496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1006-22G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1006-22G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1006-22G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.411-22G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.208-22G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1006-22G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1006-22G>T
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10932
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5265
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7526
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3361
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5321
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5497
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3971
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20798
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2379
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

15-74738592-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74738592
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74738592
    reference: chr 15
allele count: 1
allele frequency: 8.298892927683448e-6
allele num: 120498
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1006-24C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.208-24C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.411-24C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1006-24C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1006-24C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1006-24C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1006-24C>T
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5263
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5051
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4500
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20794
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1189
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

15-74740771-AAAAT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740771
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740767
    reference: chr 15
allele count: 1
allele frequency: 8.245926512302922e-6
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1192_410+1195delATTT
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1005+44_1005+47delATTT
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.207+44_207+47delATTT
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1005+44_1005+47delATTT
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1005+44_1005+47delATTT
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1005+44_1005+47delATTT
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1005+44_1005+47delATTT
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30716
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: AAAAT
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

15-74740777-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740777
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740777
    reference: chr 15
allele count: 5
allele frequency: 4.122283415229364e-5
allele num: 121292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.207+42T>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1005+42T>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1005+42T>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1005+42T>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1005+42T>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1005+42T>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1190T>A
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30716
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1260
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4173
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ

15-74740785-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740785
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740785
    reference: chr 15
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1182C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1005+34C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1005+34C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.207+34C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1005+34C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1005+34C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1005+34C>T
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3166
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30717
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1270
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52637
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

15-74740786-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740786
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740786
    reference: chr 15
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1005+33G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1005+33G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.207+33G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1005+33G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1005+33G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1005+33G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1181G>A
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30717
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3172
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4577
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52635
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

15-74740797-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740797
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740797
    reference: chr 15
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1170G>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1005+22G>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.207+22G>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1005+22G>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1005+22G>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1005+22G>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1005+22G>C
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2459
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30717
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1316
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52634
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4753
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff

15-74740803-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740803
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740803
    reference: chr 15
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1005+16G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1005+16G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.207+16G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1005+16G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1005+16G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1164G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1005+16G>A
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30717
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1322
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD

15-74740804-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740804
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740804
    reference: chr 15
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1005+15C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1163C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1005+15C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.207+15C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1005+15C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1005+15C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1005+15C>T
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30717
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52636
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1324
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4857
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

15-74740810-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740810
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740810
    reference: chr 15
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1005+9T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1005+9T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1005+9T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.207+9T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1005+9T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1005+9T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1157T>C
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30717
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4881
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

15-74740812-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740812
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740812
    reference: chr 15
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.1005+7C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1155C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.1005+7C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.1005+7C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.207+7C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.1005+7C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.1005+7C>T
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30717
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
hgvs: c.1005+7C>T
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

15-74740830-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740830
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740830
    reference: chr 15
allele count: 1
allele frequency: 8.237775141689733e-6
allele num: 121392
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.994C>T
  hgvsp: ENSP00000378518.2:p.Pro332Ser
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1137C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.994C>T
  hgvsp: ENSP00000454828.1:p.Pro332Ser
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.994C>T
  hgvsp: ENSP00000457708.1:p.Pro332Ser
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.994C>T
  hgvsp: ENSP00000354883.4:p.Pro332Ser
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.196C>T
  hgvsp: ENSP00000456662.1:p.Pro66Ser
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.994C>T
  hgvsp: ENSP00000457703.1:p.Pro332Ser
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30718
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro332Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum

15-74740832-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740832
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740832
    reference: chr 15
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.992A>G
  hgvsp: ENSP00000457708.1:p.Gln331Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.992A>G
  hgvsp: ENSP00000354883.4:p.Gln331Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.992A>G
  hgvsp: ENSP00000457703.1:p.Gln331Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.992A>G
  hgvsp: ENSP00000378518.2:p.Gln331Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.194A>G
  hgvsp: ENSP00000456662.1:p.Gln65Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.992A>G
  hgvsp: ENSP00000454828.1:p.Gln331Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1135A>G
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30717
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1333
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52635
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gln331Arg
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

15-74740834-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740834
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740834
    reference: chr 15
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.192G>A
  hgvsp: ENST00000565494.1:c.192G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.990G>A
  hgvsp: ENST00000565335.1:c.990G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.990G>A
  hgvsp: ENST00000361351.4:c.990G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.990G>A
  hgvsp: ENST00000567435.1:c.990G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.990G>A
  hgvsp: ENST00000395081.2:c.990G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.990G>A
  hgvsp: ENST00000564488.1:c.990G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1133G>A
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2382
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30717
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly330Gly
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD

15-74740849-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740849
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740849
    reference: chr 15
allele count: 5
allele frequency: 4.118412599047823e-5
allele num: 121406
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.975C>T
  hgvsp: ENST00000361351.4:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.975C>T
  hgvsp: ENST00000395081.2:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.975C>T
  hgvsp: ENST00000565335.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.975C>T
  hgvsp: ENST00000564488.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.975C>T
  hgvsp: ENST00000567435.1:c.975C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.177C>T
  hgvsp: ENST00000565494.1:c.177C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1118C>T
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3688
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30720
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1331
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala325Ala
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

15-74740853-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740853
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740853
    reference: chr 15
allele count: 1
allele frequency: 8.236689509752241e-6
allele num: 121408
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.971A>G
  hgvsp: ENSP00000457708.1:p.His324Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.971A>G
  hgvsp: ENSP00000454828.1:p.His324Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.971A>G
  hgvsp: ENSP00000457703.1:p.His324Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.971A>G
  hgvsp: ENSP00000354883.4:p.His324Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.173A>G
  hgvsp: ENSP00000456662.1:p.His58Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1114A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.971A>G
  hgvsp: ENSP00000378518.2:p.His324Arg
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30718
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1330
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4950
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52632
  bin: 9.75e1
  variant carriers: 1
hgvs: p.His324Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
reference allele: T
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ

15-74740875-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740875
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740875
    reference: chr 15
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.151C>A
  hgvsp: ENSP00000456662.1:p.Leu51Ile
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.949C>A
  hgvsp: ENSP00000454828.1:p.Leu317Ile
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.949C>A
  hgvsp: ENSP00000457703.1:p.Leu317Ile
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.949C>A
  hgvsp: ENSP00000378518.2:p.Leu317Ile
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.949C>A
  hgvsp: ENSP00000354883.4:p.Leu317Ile
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1092C>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.949C>A
  hgvsp: ENSP00000457708.1:p.Leu317Ile
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30717
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1327
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu317Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

15-74740875-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740875
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740875
    reference: chr 15
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.151C>T
  hgvsp: ENSP00000456662.1:p.Leu51Phe
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.949C>T
  hgvsp: ENSP00000454828.1:p.Leu317Phe
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1092C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.949C>T
  hgvsp: ENSP00000354883.4:p.Leu317Phe
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.949C>T
  hgvsp: ENSP00000457708.1:p.Leu317Phe
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.949C>T
  hgvsp: ENSP00000378518.2:p.Leu317Phe
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.949C>T
  hgvsp: ENSP00000457703.1:p.Leu317Phe
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2491
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30717
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1327
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu317Phe
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

15-74740880-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740880
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740880
    reference: chr 15
allele count: 25
allele frequency: 2.059104536619115e-4
allele num: 121412
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1087A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.944A>G
  hgvsp: ENSP00000457708.1:p.Asn315Ser
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.146A>G
  hgvsp: ENSP00000456662.1:p.Asn49Ser
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.944A>G
  hgvsp: ENSP00000454828.1:p.Asn315Ser
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.944A>G
  hgvsp: ENSP00000354883.4:p.Asn315Ser
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.944A>G
  hgvsp: ENSP00000378518.2:p.Asn315Ser
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.944A>G
  hgvsp: ENSP00000457703.1:p.Asn315Ser
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30721
  bin: 9.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asn315Ser
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

15-74740889-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740889
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740889
    reference: chr 15
allele count: 4
allele frequency: 3.294567258590584e-5
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.935C>T
  hgvsp: ENSP00000354883.4:p.Pro312Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1078C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.935C>T
  hgvsp: ENSP00000457708.1:p.Pro312Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.935C>T
  hgvsp: ENSP00000378518.2:p.Pro312Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.935C>T
  hgvsp: ENSP00000457703.1:p.Pro312Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.935C>T
  hgvsp: ENSP00000454828.1:p.Pro312Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.137C>T
  hgvsp: ENSP00000456662.1:p.Pro46Leu
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2486
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30714
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro312Leu
num of homozygotes: 1
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: G
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/15-74740891-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740891
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740891
    reference: chr 15
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.933G>T
  hgvsp: ENST00000395081.2:c.933G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.933G>T
  hgvsp: ENST00000567435.1:c.933G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.933G>T
  hgvsp: ENST00000565335.1:c.933G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.933G>T
  hgvsp: ENST00000361351.4:c.933G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1076G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.933G>T
  hgvsp: ENST00000564488.1:c.933G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.135G>T
  hgvsp: ENST00000565494.1:c.135G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30714
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52633
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr311Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

15-74740891-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740891
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740891
    reference: chr 15
allele count: 1
allele frequency: 8.236418146476461e-6
allele num: 121412
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.933G>A
  hgvsp: ENST00000361351.4:c.933G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.933G>A
  hgvsp: ENST00000567435.1:c.933G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.933G>A
  hgvsp: ENST00000564488.1:c.933G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.135G>A
  hgvsp: ENST00000565494.1:c.135G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1076G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.933G>A
  hgvsp: ENST00000565335.1:c.933G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.933G>A
  hgvsp: ENST00000395081.2:c.933G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2764
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3405
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1294
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2482
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30714
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52633
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr311Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ

15-74740892-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740892
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740892
    reference: chr 15
allele count: 61
allele frequency: 5.024215069350641e-4
allele num: 121412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.932C>T
  hgvsp: ENSP00000378518.2:p.Thr311Met
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.932C>T
  hgvsp: ENSP00000457708.1:p.Thr311Met
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.932C>T
  hgvsp: ENSP00000354883.4:p.Thr311Met
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.932C>T
  hgvsp: ENSP00000454828.1:p.Thr311Met
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.134C>T
  hgvsp: ENSP00000456662.1:p.Thr45Met
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.932C>T
  hgvsp: ENSP00000457703.1:p.Thr311Met
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1075C>T
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1293
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3689
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3773
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30739
  bin: 9.75e1
  variant carriers: 58
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr311Met
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

15-74740917-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740917
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740917
    reference: chr 15
allele count: 1
allele frequency: 8.237503706876667e-6
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.907A>T
  hgvsp: ENSP00000354883.4:p.Met303Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.907A>T
  hgvsp: ENSP00000378518.2:p.Met303Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.907A>T
  hgvsp: ENSP00000457703.1:p.Met303Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.907A>T
  hgvsp: ENSP00000457708.1:p.Met303Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.907A>T
  hgvsp: ENSP00000454828.1:p.Met303Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1050A>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.127-18A>T
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30717
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1318
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4947
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Met303Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD

15-74740917-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740917
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740917
    reference: chr 15
allele count: 3
allele frequency: 2.471251112063001e-5
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.127-18A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.907A>G
  hgvsp: ENSP00000457703.1:p.Met303Val
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.907A>G
  hgvsp: ENSP00000378518.2:p.Met303Val
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.907A>G
  hgvsp: ENSP00000354883.4:p.Met303Val
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.907A>G
  hgvsp: ENSP00000457708.1:p.Met303Val
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.907A>G
  hgvsp: ENSP00000454828.1:p.Met303Val
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1050A>G
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30717
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52636
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Met303Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: T
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

15-74740922-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740922
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740922
    reference: chr 15
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1045C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.902C>T
  hgvsp: ENSP00000457703.1:p.Ser301Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.127-23C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.902C>T
  hgvsp: ENSP00000354883.4:p.Ser301Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.902C>T
  hgvsp: ENSP00000378518.2:p.Ser301Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.902C>T
  hgvsp: ENSP00000454828.1:p.Ser301Leu
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.902C>T
  hgvsp: ENSP00000457708.1:p.Ser301Leu
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1834
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30715
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1314
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser301Leu
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

15-74740941-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740941
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740941
    reference: chr 15
allele count: 2
allele frequency: 1.648233917357551e-5
allele num: 121342
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.127-42G>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.883G>C
  hgvsp: ENSP00000457708.1:p.Gly295Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.883G>C
  hgvsp: ENSP00000354883.4:p.Gly295Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.883G>C
  hgvsp: ENSP00000457703.1:p.Gly295Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.883G>C
  hgvsp: ENSP00000378518.2:p.Gly295Arg
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1026G>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.883G>C
  hgvsp: ENSP00000454828.1:p.Gly295Arg
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3387
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1295
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30716
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4862
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 455
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly295Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

15-74740942-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740942
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740942
    reference: chr 15
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.883-1G>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.883-1G>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.883-1G>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1025G>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.127-43G>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.883-1G>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.883-1G>C
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1835
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30715
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2405
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1297
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
hgvs: c.883-1G>C
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ

15-74740944-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740944
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740944
    reference: chr 15
allele count: 1
allele frequency: 8.241305422778968e-6
allele num: 121340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.883-3T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.883-3T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.883-3T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.883-3T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.883-3T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1023T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.127-45T>C
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30715
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2762
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1483
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1294
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
hgvs: c.883-3T>C
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

15-74740964-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740964
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740964
    reference: chr 15
allele count: 1
allele frequency: 8.246470510621453e-6
allele num: 121264
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.883-23A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.883-23A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.883-23A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.127-65A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+1003A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.883-23A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.883-23A>G
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 702
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2082
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30714
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52634
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum

15-74740977-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740977
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740977
    reference: chr 15
allele count: 2
allele frequency: 1.650519088253256e-5
allele num: 121174
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.883-36C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.883-36C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.883-36C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.883-36C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.127-78C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+990C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.883-36C>T
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1788
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 713
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30714
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1296
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52628
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

15-74740986-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740986
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740986
    reference: chr 15
allele count: 580
allele frequency: 4.789113848796116e-3
allele num: 121108
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.883-45T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.883-45T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.883-45T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.127-87T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+981T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.883-45T>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.883-45T>C
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1728
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 3.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3767
  bin: 9.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1811
  bin: 2.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 3662
  bin: 8.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2366
  bin: 7.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2747
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 30831
  bin: 9.75e1
  variant carriers: 418
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 8.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 2025
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52673
  bin: 9.75e1
  variant carriers: 563
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 16
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: A
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

15-74740992-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74740992
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74740992
    reference: chr 15
allele count: 3
allele frequency: 2.479133955871415e-5
allele num: 121010
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.883-51A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.883-51A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.883-51A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+975A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.883-51A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.127-93A>G
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.883-51A>G
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1833
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3780
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3686
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30756
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 888
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: VQSLOD

15-74741481-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74741481
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74741481
    reference: chr 15
allele count: 1
allele frequency: 9.307173969695841e-6
allele num: 107444
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.882+46C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+486C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.882+46C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.882+46C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.126+46C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.882+46C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.882+46C>T
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10316
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 737
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35274
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7486
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/15-74741484-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74741484
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74741484
    reference: chr 15
allele count: 2
allele frequency: 1.862266751089426e-5
allele num: 107396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.882+43G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.882+43G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.882+43G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.126+43G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.882+43G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+483G>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.882+43G>T
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4340
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10325
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10383
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27129
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3367
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2061
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2191
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 567
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 732
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1261
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

15-74741485-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74741485
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74741485
    reference: chr 15
allele count: 1
allele frequency: 9.31237428294718e-6
allele num: 107384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.882+42G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.882+42G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.882+42G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+482G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.882+42G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.882+42G>A
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.126+42G>A
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4346
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10314
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 568
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 594
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3430
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2062
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7464
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1255
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

15-74741486-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74741486
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74741486
    reference: chr 15
allele count: 1
allele frequency: 9.309773400115442e-6
allele num: 107414
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.126+41A>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.882+41A>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+481A>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.882+41A>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.882+41A>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.882+41A>C
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.882+41A>C
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1946
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4351
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10326
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3469
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1477
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2067
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 719
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD

15-74741492-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 74741492
    reference: chr 15
  end: Position
    type: ExactPosition
    position: 74741492
    reference: chr 15
allele count: 98
allele frequency: 9.125107080338188e-4
allele num: 107396
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457703
  ensembl transcript: ENST00000567435
  gene symbol: UBL7
  hgvsc: ENST00000567435.1:c.882+35C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456662
  ensembl transcript: ENST00000565494
  gene symbol: UBL7
  hgvsc: ENST00000565494.1:c.126+35C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000378518
  ensembl transcript: ENST00000395081
  gene symbol: UBL7
  hgvsc: ENST00000395081.2:c.882+35C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000454828
  ensembl transcript: ENST00000564488
  gene symbol: UBL7
  hgvsc: ENST00000564488.1:c.882+35C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000457708
  ensembl transcript: ENST00000565335
  gene symbol: UBL7
  hgvsc: ENST00000565335.1:c.882+35C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000354883
  ensembl transcript: ENST00000361351
  gene symbol: UBL7
  hgvsc: ENST00000361351.4:c.882+35C>T
  variant of: http://identifiers.org/hgnc/28221
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000138629
  ensembl protein: ENSP00000456807
  ensembl transcript: ENST00000566365
  gene symbol: UBL7
  hgvsc: ENST00000566365.1:c.410+475C>T
  variant of: http://identifiers.org/hgnc/28221
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 941
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10340
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27324
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4295
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 10639
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 6.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2040
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2130
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36190
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 7440
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1293
  bin: 9.75e1
  variant carriers: 95
num of homozygotes: 1
population: European (Finnish)
reference allele: G

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.2732e4

VQSLOD
type: SiteQuality
SIO_000300: -1.175e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.31e-1

QD
type: SiteQuality
SIO_000300: 7.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.859999999999999e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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South Asian
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Latino
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European (Non-Finnish)
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African
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European (Finnish)
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Other
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MQ
type: SiteQuality
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QD
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InbreedingCoeff
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FS
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DP
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VQSLOD
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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Other
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European (Non-Finnish)
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allele frequency: 2.173913043478261e-2
allele num: 46
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Latino
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East Asian
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MQ
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InbreedingCoeff
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ClippingRankSum
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FS
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QD
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MQRankSum
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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DP
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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European (Finnish)
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Latino
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Other
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East Asian
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InbreedingCoeff
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QD
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FS
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VQSLOD
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MQ
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ReadPosRankSum
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DP
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MQRankSum
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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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Other
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European (Non-Finnish)
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South Asian
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European (Finnish)
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East Asian
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African
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Latino
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QD
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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DP
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BaseQRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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South Asian
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allele frequency: 7.003692856233286e-4
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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Other
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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MQ
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SIO_000300: 5.967e1

InbreedingCoeff
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VQSLOD
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FS
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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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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European (Finnish)
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allele num: 6586
num of homozygotes: 0

African
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South Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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East Asian
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allele frequency: 4.68384074941452e-4
allele num: 8540
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Latino
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Other
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InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 4.4e-1

BaseQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 5.79e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.203004e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-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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African
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allele num: 10244
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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
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European (Non-Finnish)
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allele frequency: 1.509980974239725e-5
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Latino
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European (Finnish)
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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QD
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MQ
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FS
type: SiteQuality
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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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European (Non-Finnish)
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allele frequency: 4.527481814614711e-5
allele num: 66262
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Latino
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South Asian
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African
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European (Finnish)
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Other
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East Asian
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InbreedingCoeff
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DP
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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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VQSLOD
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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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South Asian
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Latino
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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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VQSLOD
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MQ
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BaseQRankSum
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MQRankSum
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DP
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InbreedingCoeff
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QD
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FS
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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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African
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Other
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European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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VQSLOD
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BaseQRankSum
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DP
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MQ
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ClippingRankSum
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InbreedingCoeff
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FS
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ReadPosRankSum
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QD
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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African
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Other
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European (Finnish)
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South Asian
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ClippingRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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QD
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MQRankSum
type: SiteQuality
SIO_000300: -2.94e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e0

DP
type: SiteQuality
SIO_000300: 2.245536e6

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
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

QD
type: SiteQuality
SIO_000300: 1.208e1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e-1

DP
type: SiteQuality
SIO_000300: 2.246733e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.497e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.34e0

MQ
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 5.68e0

VQSLOD
type: SiteQuality
SIO_000300: 1.19e-1

GenotypeQuality
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bin: 8.25e1
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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bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504936190705514e-5
allele num: 66448
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

QD
type: SiteQuality
SIO_000300: 1.004e1

DP
type: SiteQuality
SIO_000300: 2.247347e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.162e0

VQSLOD
type: SiteQuality
SIO_000300: 4.91e-1

GenotypeQuality
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variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66458
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: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.959e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

VQSLOD
type: SiteQuality
SIO_000300: 7.39e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.099e0

MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 4.17e0

QD
type: SiteQuality
SIO_000300: 1.015e1

DP
type: SiteQuality
SIO_000300: 2.247458e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.43e-1

GenotypeQuality
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variant carriers: 0

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.505026789476853e-5
allele num: 66444
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 1.5682e1

DP
type: SiteQuality
SIO_000300: 2.247569e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.329e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.17e-1

QD
type: SiteQuality
SIO_000300: 1.225e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

MQRankSum
type: SiteQuality
SIO_000300: -3.9e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.372e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.522643155899256e-5
allele num: 66466
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10326
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.062075654704171e-5
allele num: 16496
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 1.189e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.248113e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

MQ
type: SiteQuality
SIO_000300: 5.937e1

MQRankSum
type: SiteQuality
SIO_000300: 4.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8618
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.67305088024763e-5
allele num: 10338
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66494
num of homozygotes: 0

European (Finnish)
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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: 902
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South Asian
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allele count: 0
allele frequency: 0.0e0
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e-1

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.248228e6

MQ
type: SiteQuality
SIO_000300: 5.839e1

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.723e0

MQRankSum
type: SiteQuality
SIO_000300: 7.26e-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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African
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allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

Other
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allele num: 902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.007790176557283e-5
allele num: 66494
num of homozygotes: 0

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

Latino
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South Asian
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MQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
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InbreedingCoeff
type: SiteQuality
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QD
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VQSLOD
type: SiteQuality
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BaseQRankSum
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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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
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African
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allele count: 1
allele frequency: 9.665571235260003e-5
allele num: 10346
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South Asian
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.504121292341014e-5
allele num: 66484
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.71e-1

InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e-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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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.503397678753984e-5
allele num: 66516
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Other
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele num: 6608
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MQ
type: SiteQuality
SIO_000300: 5.952e1

FS
type: SiteQuality
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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DP
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MQRankSum
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ReadPosRankSum
type: SiteQuality
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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
all individuals: 18966
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 6224
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2923
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.592912705272256e-4
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007066606525334e-5
allele num: 66510
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.31696014828545e-4
allele num: 8632
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: 6608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.39e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.08e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.943e1

DP
type: SiteQuality
SIO_000300: 2.24897e6

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

GenotypeQuality
all individuals: 4529
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16299
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2923
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18960
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6230
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3969
bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66512
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10354
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.158480074142725e-4
allele num: 8632
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.25e-1

QD
type: SiteQuality
SIO_000300: 1.552e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.651e0

DP
type: SiteQuality
SIO_000300: 2.24836e6

MQ
type: SiteQuality
SIO_000300: 5.951e1

VQSLOD
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.57e0

GenotypeQuality
all individuals: 174
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6173
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3965
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2376
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2916
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4775
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15821
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4523
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.898550724637681e-4
allele num: 10350
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66508
num of homozygotes: 0

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

QD
type: SiteQuality
SIO_000300: 1.254e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.36e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.68e-1

FS
type: SiteQuality
SIO_000300: 5.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.61e-1

DP
type: SiteQuality
SIO_000300: 2.244471e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

GenotypeQuality
all individuals: 183
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4524
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2378
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variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4774
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variant carriers: 0

GenotypeQuality
all individuals: 3965
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6164
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18959
bin: 9.75e1
variant carriers: 3

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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: 10346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007609251406057e-5
allele num: 66498
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.964e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.02e-1

QD
type: SiteQuality
SIO_000300: 1.138e1

DP
type: SiteQuality
SIO_000300: 2.24396e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

FS
type: SiteQuality
SIO_000300: 4.193e0

MQRankSum
type: SiteQuality
SIO_000300: 8.37e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

GenotypeQuality
all individuals: 691
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5874
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variant carriers: 0

GenotypeQuality
all individuals: 3959
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variant carriers: 0

GenotypeQuality
all individuals: 224
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2369
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4498
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variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18956
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4720
bin: 7.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66406
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.728907330567082e-4
allele num: 11568
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -3.255e0

QD
type: SiteQuality
SIO_000300: 1.255e1

FS
type: SiteQuality
SIO_000300: 6.35e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.29e-1

DP
type: SiteQuality
SIO_000300: 2.23614e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.1e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.14e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

GenotypeQuality
all individuals: 3952
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 502
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 150
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14235
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2366
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 298
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 592
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4678
bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.773260359655981e-5
allele num: 10232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.538935056940597e-4
allele num: 6498
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66080
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.7638e1

MQ
type: SiteQuality
SIO_000300: 5.975e1

VQSLOD
type: SiteQuality
SIO_000300: -2.701e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

DP
type: SiteQuality
SIO_000300: 2.234611e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.83e0

QD
type: SiteQuality
SIO_000300: 1.45e0

GenotypeQuality
all individuals: 306
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19345
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 207
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2912
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2421
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14553
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4884
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4096
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.75e1
variant carriers: 0

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

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505072092953252e-5
allele num: 66442
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.06e-1

DP
type: SiteQuality
SIO_000300: 2.256401e6

MQRankSum
type: SiteQuality
SIO_000300: -4.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 2.499e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

QD
type: SiteQuality
SIO_000300: 1.156e1

MQ
type: SiteQuality
SIO_000300: 5.976e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.319e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

GenotypeQuality
all individuals: 5889
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4675
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 207
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19345
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 82
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4096
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 5.25e1
variant carriers: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.116071428571429e-3
allele num: 896
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10338
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66442
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.156e1

FS
type: SiteQuality
SIO_000300: 2.499e0

DP
type: SiteQuality
SIO_000300: 2.256401e6

MQRankSum
type: SiteQuality
SIO_000300: -4.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 9.06e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.319e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

GenotypeQuality
all individuals: 13840
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2814
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 3824
bin: 9.25e1
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GenotypeQuality
all individuals: 154
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 214
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 7.5e0
variant carriers: 3

GenotypeQuality
all individuals: 4521
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 172
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 185
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2700
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 560
bin: 2.25e1
variant carriers: 2

African
type: Population
allele count: 4
allele frequency: 4.276245456489202e-4
allele num: 9354
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.751313485113835e-4
allele num: 11420
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.086427267194157e-5
allele num: 16430
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.540240736370073e-4
allele num: 8474
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 16
allele frequency: 2.943340691685063e-3
allele num: 5436
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.487562189054726e-3
allele num: 804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 37
allele frequency: 5.90771195912502e-4
allele num: 62630
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.352e0

DP
type: SiteQuality
SIO_000300: 2.294012e6

VQSLOD
type: SiteQuality
SIO_000300: -8.115000000000001e1

MQ
type: SiteQuality
SIO_000300: 5.917e1

FS
type: SiteQuality
SIO_000300: 1.30586e2

QD
type: SiteQuality
SIO_000300: 9.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.78e0

MQRankSum
type: SiteQuality
SIO_000300: 3.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.662e0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4712
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2828
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4520
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14419
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
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variant carriers: 0

GenotypeQuality
all individuals: 618
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.75e1
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GenotypeQuality
all individuals: 20819
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3973
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2383
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66454
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.729206294310911e-4
allele num: 11566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 2.271552e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.16e-1

QD
type: SiteQuality
SIO_000300: 1.173e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.78e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

FS
type: SiteQuality
SIO_000300: 1.408e0

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

MQRankSum
type: SiteQuality
SIO_000300: -9.7e-2

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2383
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2812
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5584
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3972
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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: 10352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505978735580254e-5
allele num: 66402
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16226
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.830000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.265957e6

MQ
type: SiteQuality
SIO_000300: 5.932e1

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -1.313e0

FS
type: SiteQuality
SIO_000300: 1.351e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.19e0

QD
type: SiteQuality
SIO_000300: 6.59e0

GenotypeQuality
all individuals: 165
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2383
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4700
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2808
bin: 7.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.659969088098918e-5
allele num: 10352
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: 11564
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.205000753125471e-4
allele num: 66390
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.5e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.144e0

FS
type: SiteQuality
SIO_000300: 1.485e0

DP
type: SiteQuality
SIO_000300: 2.263603e6

MQRankSum
type: SiteQuality
SIO_000300: 7.099999999999999e-2

MQ
type: SiteQuality
SIO_000300: 5.972e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e-1

QD
type: SiteQuality
SIO_000300: 1.175e1

GenotypeQuality
all individuals: 2812
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 13750
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5557
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4696
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variant carriers: 0

GenotypeQuality
all individuals: 20811
bin: 9.75e1
variant carriers: 2

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16188
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.506205566935775e-5
allele num: 66392
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.9e-1

QD
type: SiteQuality
SIO_000300: 9.630000000000001e0

DP
type: SiteQuality
SIO_000300: 2.263357e6

FS
type: SiteQuality
SIO_000300: 4.526e0

VQSLOD
type: SiteQuality
SIO_000300: 5.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

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

GenotypeQuality
all individuals: 126
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4503
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1080
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variant carriers: 0

GenotypeQuality
all individuals: 4679
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2783
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13155
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.898550724637681e-4
allele num: 10350
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: 16098
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66340
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.67e0

DP
type: SiteQuality
SIO_000300: 2.255891e6

MQRankSum
type: SiteQuality
SIO_000300: 3.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.355e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

QD
type: SiteQuality
SIO_000300: 1.571e1

GenotypeQuality
all individuals: 149
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5445
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12713
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 493
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3970
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2379
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variant carriers: 0

GenotypeQuality
all individuals: 2771
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16104
num of homozygotes: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.66183574879227e-5
allele num: 10350
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66338
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.18e0

DP
type: SiteQuality
SIO_000300: 2.250463e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

QD
type: SiteQuality
SIO_000300: 1.31e1

FS
type: SiteQuality
SIO_000300: 2.796e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.36e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.084e0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
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variant carriers: 0

GenotypeQuality
all individuals: 129
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3783
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 2.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66654
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.297e1

FS
type: SiteQuality
SIO_000300: 9.795999999999999e0

DP
type: SiteQuality
SIO_000300: 5.723274e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

VQSLOD
type: SiteQuality
SIO_000300: 6.96e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.661e0

MQ
type: SiteQuality
SIO_000300: 5.419e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.282e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 96
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GenotypeQuality
all individuals: 273
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52639
bin: 9.75e1
variant carriers: 5

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

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

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

African
type: Population
allele count: 5
allele frequency: 4.806767929244376e-4
allele num: 10402
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 6.98e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.381e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.87e-1

DP
type: SiteQuality
SIO_000300: 5.725267e6

QD
type: SiteQuality
SIO_000300: 1.3e1

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 2.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.41e0

DP
type: SiteQuality
SIO_000300: 5.728307e6

VQSLOD
type: SiteQuality
SIO_000300: 3.15e-1

QD
type: SiteQuality
SIO_000300: 1.278e1

MQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-2

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.68e-1

GenotypeQuality
all individuals: 271
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 356
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GenotypeQuality
all individuals: 84
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variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 446
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GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 47
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GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 8.75e1
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GenotypeQuality
all individuals: 1259
bin: 6.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06501698204755e-5
allele num: 16488
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 8.874000000000001e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

DP
type: SiteQuality
SIO_000300: 5.728994e6

BaseQRankSum
type: SiteQuality
SIO_000300: -5.23e0

QD
type: SiteQuality
SIO_000300: 1.166e1

MQ
type: SiteQuality
SIO_000300: 5.955e1

VQSLOD
type: SiteQuality
SIO_000300: -9.14e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -2.03e-1

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

GenotypeQuality
all individuals: 47
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 359
bin: 8.25e1
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GenotypeQuality
all individuals: 266
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 904
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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 count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

MQ
type: SiteQuality
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QD
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DP
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ClippingRankSum
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SIO_000300: -3.78e-1

FS
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BaseQRankSum
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.1e-3

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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bin: 5.75e1
variant carriers: 0

Latino
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allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQRankSum
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VQSLOD
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DP
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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SIO_000300: 6.707e0

MQ
type: SiteQuality
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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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variant carriers: 0

East Asian
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allele frequency: 0.0e0
allele num: 8652
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10402
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

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

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

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

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

Latino
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allele num: 11578
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East Asian
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allele num: 8652
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: 906
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

MQ
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
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SIO_000300: 7.06e0

MQRankSum
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QD
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SIO_000300: 1.495e1

InbreedingCoeff
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DP
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VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: 7.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-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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bin: 5.25e1
variant carriers: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997871511227029e-5
allele num: 66714
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

QD
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SIO_000300: 1.25e1

MQRankSum
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InbreedingCoeff
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SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.332e0

VQSLOD
type: SiteQuality
SIO_000300: 9.84e-1

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.63e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.3e-2

DP
type: SiteQuality
SIO_000300: 5.732207e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.3e0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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DP
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InbreedingCoeff
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SIO_000300: -2.0e-4

QD
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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BaseQRankSum
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FS
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ClippingRankSum
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SIO_000300: 1.62e-1

MQ
type: SiteQuality
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MQRankSum
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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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
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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: 906
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498486528606108e-5
allele num: 66734
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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DP
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MQ
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ClippingRankSum
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InbreedingCoeff
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FS
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VQSLOD
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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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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 5.993586862057598e-5
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num of homozygotes: 0

East Asian
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Latino
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African
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European (Finnish)
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South Asian
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VQSLOD
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FS
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MQ
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QD
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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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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East Asian
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European (Finnish)
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South Asian
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Latino
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Other
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European (Non-Finnish)
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allele frequency: 1.4983967155144e-5
allele num: 66738
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African
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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FS
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VQSLOD
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DP
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InbreedingCoeff
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QD
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MQ
type: SiteQuality
SIO_000300: 5.988e1

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

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52632
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.733134e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.99e-1

QD
type: SiteQuality
SIO_000300: 1.1e1

FS
type: SiteQuality
SIO_000300: 1.761e0

VQSLOD
type: SiteQuality
SIO_000300: 7.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.488e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-2

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

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
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: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.761e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.99e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.07e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-2

QD
type: SiteQuality
SIO_000300: 1.1e1

DP
type: SiteQuality
SIO_000300: 5.733134e6

VQSLOD
type: SiteQuality
SIO_000300: 7.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.488e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 25

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 165
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variant carriers: 0

GenotypeQuality
all individuals: 4964
bin: 6.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 5
allele frequency: 4.318535152876144e-4
allele num: 11578
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.804920238324044e-4
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 1.947857356907402e-4
allele num: 66740
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 5.736624e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.431e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.9e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.73e0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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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variant carriers: 0

GenotypeQuality
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variant carriers: 3

GenotypeQuality
all individuals: 520
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variant carriers: 0

GenotypeQuality
all individuals: 469
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variant carriers: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.422480620155039e-4
allele num: 16512
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
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

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

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

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

QD
type: SiteQuality
SIO_000300: 1.363e1

MQ
type: SiteQuality
SIO_000300: 5.966e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.45e0

MQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.820000000000001e-1

FS
type: SiteQuality
SIO_000300: 3.233e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.28e-1

DP
type: SiteQuality
SIO_000300: 5.732919e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.817e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

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

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 519
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variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 8.75e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 5.27e-1

QD
type: SiteQuality
SIO_000300: 1.136e1

DP
type: SiteQuality
SIO_000300: 5.73287e6

VQSLOD
type: SiteQuality
SIO_000300: 2.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

GenotypeQuality
all individuals: 4
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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: 519
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variant carriers: 0

GenotypeQuality
all individuals: 1325
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variant carriers: 0

GenotypeQuality
all individuals: 265
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 165
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variant carriers: 0

GenotypeQuality
all individuals: 4958
bin: 6.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.72e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.46e-1

DP
type: SiteQuality
SIO_000300: 5.73287e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e0

QD
type: SiteQuality
SIO_000300: 1.136e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

GenotypeQuality
all individuals: 471
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 61

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1324
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 9
allele frequency: 7.77336327517706e-4
allele num: 11578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 50
allele frequency: 4.804920238324044e-3
allele num: 10406
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.94e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

QD
type: SiteQuality
SIO_000300: 1.335e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e0

DP
type: SiteQuality
SIO_000300: 5.743361e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 52636
bin: 9.75e1
variant carriers: 1

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: 16512
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.64e-1

FS
type: SiteQuality
SIO_000300: 3.549e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.37e0

DP
type: SiteQuality
SIO_000300: 5.733008e6

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

QD
type: SiteQuality
SIO_000300: 1.455e1

GenotypeQuality
all individuals: 4947
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1318
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GenotypeQuality
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GenotypeQuality
all individuals: 19
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 5.733008e6

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 8.64e-1

MQ
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.3e-1

QD
type: SiteQuality
SIO_000300: 1.455e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 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: 908
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.92e-1

QD
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SIO_000300: 1.079e1

DP
type: SiteQuality
SIO_000300: 5.732355e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.829e0

MQRankSum
type: SiteQuality
SIO_000300: -1.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.6e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

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

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

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

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

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

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

South Asian
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allele count: 2
allele frequency: 1.211680600993578e-4
allele num: 16506
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.73e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.291e1

VQSLOD
type: SiteQuality
SIO_000300: -1.048e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.679e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 5.821e0

DP
type: SiteQuality
SIO_000300: 5.731448e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10400
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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.44e-1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.046e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 5.731296e6

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

FS
type: SiteQuality
SIO_000300: 1.742e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.338e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
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: 10400
num of homozygotes: 0

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 5.731177e6

MQ
type: SiteQuality
SIO_000300: 5.947e1

VQSLOD
type: SiteQuality
SIO_000300: -8.37e-2

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.039e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.012e0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.17e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.79e-1

GenotypeQuality
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bin: 1.75e1
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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variant carriers: 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: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8652
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.283e0

QD
type: SiteQuality
SIO_000300: 1.362e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -7.186e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

DP
type: SiteQuality
SIO_000300: 5.723938e6

MQRankSum
type: SiteQuality
SIO_000300: -1.097e0

GenotypeQuality
all individuals: 493
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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
all individuals: 916
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GenotypeQuality
all individuals: 207
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501411326647048e-5
allele num: 66604
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e-1

QD
type: SiteQuality
SIO_000300: 1.401e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.485e0

FS
type: SiteQuality
SIO_000300: 2.076e0

MQRankSum
type: SiteQuality
SIO_000300: 2.27e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 2.07e0

DP
type: SiteQuality
SIO_000300: 5.709963e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-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
all individuals: 304
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GenotypeQuality
all individuals: 400
bin: 5.25e1
variant carriers: 1

Latino
type: Population
allele count: 3
allele frequency: 2.592464569650881e-4
allele num: 11572
num of homozygotes: 0

East Asian
type: Population
allele count: 521
allele frequency: 6.031488770548738e-2
allele num: 8638
num of homozygotes: 16

European (Non-Finnish)
type: Population
allele count: 21
allele frequency: 3.154195079455676e-4
allele num: 66578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 12
allele frequency: 1.814333232537043e-3
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 17
allele frequency: 1.036206266000244e-3
allele num: 16406
num of homozygotes: 0

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

Other
type: Population
allele count: 6
allele frequency: 6.622516556291391e-3
allele num: 906
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.975e1

QD
type: SiteQuality
SIO_000300: 1.64e1

DP
type: SiteQuality
SIO_000300: 5.709287e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.0e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.71e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.55e0

MQRankSum
type: SiteQuality
SIO_000300: 2.72e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.25e0

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503171692270691e-5
allele num: 66526
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.223241590214067e-4
allele num: 16350
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 6.51e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.26e-1

FS
type: SiteQuality
SIO_000300: 1.206e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.092e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.794e1

VQSLOD
type: SiteQuality
SIO_000300: -1.579e-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
all individuals: 2221
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9240
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6434
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.610669071932481e-5
allele num: 62086
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8990
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MQ
type: SiteQuality
SIO_000300: 5.947e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.486311e6

FS
type: SiteQuality
SIO_000300: 2.208e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.19e-1

QD
type: SiteQuality
SIO_000300: 1.775e1

MQRankSum
type: SiteQuality
SIO_000300: -4.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.39e-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
all individuals: 577
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6422
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9224
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9000
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.222791582068388e-5
allele num: 62058
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 6.521e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.487443e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.251e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: -6.637999999999999e-1

GenotypeQuality
all individuals: 418
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35708
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1432
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2191
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1139
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.611447724635813e-5
allele num: 62056
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6424
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8996
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9218
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

FS
type: SiteQuality
SIO_000300: 4.865e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.06e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.35e-1

QD
type: SiteQuality
SIO_000300: 1.007e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.28e-1

DP
type: SiteQuality
SIO_000300: 1.487888e6

GenotypeQuality
all individuals: 478
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2189
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 422
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35901
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 390
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1143
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7464
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 9.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6434
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9224
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8996
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.736676568233443e-5
allele num: 11446
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

DP
type: SiteQuality
SIO_000300: 1.488254e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.747e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.263e1

GenotypeQuality
all individuals: 1667
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1108
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 519
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3513
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 230
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 8.75e1
variant carriers: 0

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