16-4659593-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659593
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659593
    reference: chr 16
allele count: 3
allele frequency: 5.227573708789294e-5
allele num: 57388
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*391G>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-540G>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.*41G>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.*41G>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.*41G>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.*41G>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.*41G>C
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15382
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17360
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7936
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5578
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6403
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4659
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2052
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4611
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD

16-4659597-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659597
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659597
    reference: chr 16
allele count: 4
allele frequency: 6.921852287672181e-5
allele num: 57788
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.*37G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*387G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.*37G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.*37G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.*37G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.*37G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-544G>A
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8313
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7453
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4311
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
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genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1671
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.5e0
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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: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1266
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

16-4659598-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659598
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659598
    reference: chr 16
allele count: 3
allele frequency: 5.162800302884284e-5
allele num: 58108
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.*36C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.*36C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-545C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*386C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.*36C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.*36C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.*36C>T
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9176
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6192
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 5.75e1
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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: 176
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9028
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

16-4659601-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659601
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659601
    reference: chr 16
allele count: 1
allele frequency: 1.691932864103952e-5
allele num: 59104
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.*33C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*383C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.*33C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.*33C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.*33C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.*33C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-548C>T
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 10
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1077
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4426
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1149
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD

16-4659605-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659605
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659605
    reference: chr 16
allele count: 24
allele frequency: 3.997068816201452e-4
allele num: 60044
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.*29A>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.*29A>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.*29A>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.*29A>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-552A>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*379A>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.*29A>G
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17749
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2256
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 12737
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11851
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6348
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3047
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1230
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16690
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1107
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5442
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4328
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

16-4659612-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659612
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659612
    reference: chr 16
allele count: 201
allele frequency: 3.22208329325767e-3
allele num: 62382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.*22G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.*22G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.*22G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.*22G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-559G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*372G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.*22G>A
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 3.25e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2399
  bin: 1.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 17165
  bin: 7.5e0
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3070
  bin: 2.75e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5644
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10510
  bin: 1.25e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15099
  bin: 2.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4537
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 834
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16477
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 951
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 9.75e1
  variant carriers: 202
genotype quality: GenotypeQuality
  all individuals: 3774
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 7.75e1
  variant carriers: 4
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum

16-4659613-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659613
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659613
    reference: chr 16
allele count: 5
allele frequency: 7.876992879198437e-5
allele num: 63476
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.*21C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.*21C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.*21C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-560C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.*21C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*371C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.*21C>T
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  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: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5489
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16926
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3355
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15749
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9978
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3659
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2312
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4318
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 972
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1569
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4690
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16176
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ

16-4659614-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659614
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659614
    reference: chr 16
allele count: 1
allele frequency: 1.552409339294585e-5
allele num: 64416
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*370C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.*20C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.*20C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-561C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.*20C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.*20C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.*20C>T
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16322
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16762
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5417
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2185
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16237
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 16690
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 783
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 653
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

16-4659616-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659616
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659616
    reference: chr 16
allele count: 3
allele frequency: 4.580572266161786e-5
allele num: 65494
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.*18T>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.*18T>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*368T>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.*18T>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-563T>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.*18T>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.*18T>A
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8838
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5189
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15903
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3244
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1952
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4600
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

16-4659616-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659616
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659615
    reference: chr 16
allele count: 2
allele frequency: 3.053714844107857e-5
allele num: 65494
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.*17delC
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.*17delC
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.*17delC
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*367delC
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.*17delC
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-564delC
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.*17delC
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5189
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8838
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16241
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17620
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3244
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 644
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1952
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4600
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: AG
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

16-4659617-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659617
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659617
    reference: chr 16
allele count: 1
allele frequency: 1.505751972535084e-5
allele num: 66412
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.*17C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-564C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*367C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.*17C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.*17C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.*17C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.*17C>A
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16020
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3115
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3491
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4595
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15903
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

16-4659617-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659617
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659617
    reference: chr 16
allele count: 2
allele frequency: 3.011503945070168e-5
allele num: 66412
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-564C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.*17C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.*17C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.*17C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*367C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.*17C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.*17C>T
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4009
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8342
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16020
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15903
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 598
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1844
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3491
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1855
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 713
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 566
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-4659618-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659618
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659618
    reference: chr 16
allele count: 2
allele frequency: 2.974773917182294e-5
allele num: 67232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-565C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.*16C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*366C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.*16C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.*16C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.*16C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.*16C>T
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15793
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7890
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19177
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 547
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4545
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3288
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1908
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 588
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

16-4659618-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659618
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659618
    reference: chr 16
allele count: 4
allele frequency: 5.949547834364588e-5
allele num: 67232
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*366C>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.*16C>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-565C>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.*16C>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.*16C>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.*16C>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.*16C>G
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7890
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15793
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19177
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2985
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4545
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15716
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 3288
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

16-4659618-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659618
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659618
    reference: chr 16
allele count: 3
allele frequency: 4.462160875773441e-5
allele num: 67232
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.*16C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-565C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.*16C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.*16C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.*16C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*366C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.*16C>A
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5039
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15793
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7890
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19177
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4126
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1742
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20470
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4545
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15716
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-4659621-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659621
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659621
    reference: chr 16
allele count: 3
allele frequency: 4.302802558733255e-5
allele num: 69722
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.*13C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.*13C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.*13C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.*13C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*363C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-568C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.*13C>T
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 831
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4852
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21064
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6881
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14993
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 343
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2831
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2629
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22473
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15023
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-4659633-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659633
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659633
    reference: chr 16
allele count: 1
allele frequency: 1.237164419151305e-5
allele num: 80830
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*351G>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.*1G>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.*1G>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.*1G>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.*1G>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-580G>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.*1G>C
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28523
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 922
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10652
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 321
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2745
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3863
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

16-4659644-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659644
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659644
    reference: chr 16
allele count: 3
allele frequency: 3.407000249846685e-5
allele num: 88054
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.449C>T
  hgvsp: ENSP00000466404.1:p.Ala150Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.461C>T
  hgvsp: ENSP00000467671.1:p.Ala154Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-591C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.524C>T
  hgvsp: ENSP00000283474.6:p.Ala175Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*340C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.344C>T
  hgvsp: ENSP00000464725.1:p.Ala115Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.629C>T
  hgvsp: ENSP00000465706.1:p.Ala210Val
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7605
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3866
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32632
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7190
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3052
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35842
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 440
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala175Val
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum

16-4659651-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659651
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659651
    reference: chr 16
allele count: 3
allele frequency: 3.288464068049283e-5
allele num: 91228
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.517A>G
  hgvsp: ENSP00000283474.6:p.Met173Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.454A>G
  hgvsp: ENSP00000467671.1:p.Met152Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.337A>G
  hgvsp: ENSP00000464725.1:p.Met113Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-598A>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.622A>G
  hgvsp: ENSP00000465706.1:p.Met208Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.442A>G
  hgvsp: ENSP00000466404.1:p.Met148Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*333A>G
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3795
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33962
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6171
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  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: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7838
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 694
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3281
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3515
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6035
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Met173Val
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-4659659-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659659
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659659
    reference: chr 16
allele count: 15
allele frequency: 1.621130900916479e-4
allele num: 92528
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.434A>C
  hgvsp: ENSP00000466404.1:p.His145Pro
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.509A>C
  hgvsp: ENSP00000283474.6:p.His170Pro
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-606A>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.329A>C
  hgvsp: ENSP00000464725.1:p.His110Pro
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.446A>C
  hgvsp: ENSP00000467671.1:p.His149Pro
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*325A>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.614A>C
  hgvsp: ENSP00000465706.1:p.His205Pro
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8621
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3698
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4987
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 33890
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  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: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3267
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3398
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 8.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 633
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 37817
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 4.25e1
  variant carriers: 1
hgvs: p.His170Pro
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQ

16-4659669-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659669
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659669
    reference: chr 16
allele count: 1
allele frequency: 1.04331858776396e-5
allele num: 95848
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.319C>T
  hgvsp: ENSP00000464725.1:p.Pro107Ser
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*315C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.436C>T
  hgvsp: ENSP00000467671.1:p.Pro146Ser
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.499C>T
  hgvsp: ENSP00000283474.6:p.Pro167Ser
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-616C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.604C>T
  hgvsp: ENSP00000465706.1:p.Pro202Ser
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.424C>T
  hgvsp: ENSP00000466404.1:p.Pro142Ser
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9422
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3790
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1893
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 3.75e1
  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: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3505
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 727
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro167Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-4659679-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659679
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659679
    reference: chr 16
allele count: 1
allele frequency: 1.028954787726627e-5
allele num: 97186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.426C>A
  hgvsp: ENST00000591401.1:c.426C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*305C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.594C>A
  hgvsp: ENST00000590891.1:c.594C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.489C>A
  hgvsp: ENST00000283474.7:c.489C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.414C>A
  hgvsp: ENST00000587615.1:c.414C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.309C>A
  hgvsp: ENST00000591897.1:c.309C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-626C>A
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  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: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3862
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3433
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 393
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41066
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala163Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

16-4659680-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659680
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659680
    reference: chr 16
allele count: 1
allele frequency: 1.028467994076024e-5
allele num: 97232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.413C>T
  hgvsp: ENSP00000466404.1:p.Ala138Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.308C>T
  hgvsp: ENSP00000464725.1:p.Ala103Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*304C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.425C>T
  hgvsp: ENSP00000467671.1:p.Ala142Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.488C>T
  hgvsp: ENSP00000283474.6:p.Ala163Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-627C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.593C>T
  hgvsp: ENSP00000465706.1:p.Ala198Val
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3747
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9840
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41122
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3590
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala163Val
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

16-4659684-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659684
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659684
    reference: chr 16
allele count: 56
allele frequency: 5.739586749754018e-4
allele num: 97568
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*300C>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.589C>G
  hgvsp: ENSP00000465706.1:p.Gln197Glu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.409C>G
  hgvsp: ENSP00000466404.1:p.Gln137Glu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.421C>G
  hgvsp: ENSP00000467671.1:p.Gln141Glu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.304C>G
  hgvsp: ENSP00000464725.1:p.Gln102Glu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-631C>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.484C>G
  hgvsp: ENSP00000283474.6:p.Gln162Glu
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1132
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 34999
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1992
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3428
  bin: 7.5e0
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 759
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3571
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3894
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3493
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln162Glu
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

16-4659685-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659685
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659685
    reference: chr 16
allele count: 2
allele frequency: 2.048424761358515e-5
allele num: 97636
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.483A>G
  hgvsp: ENST00000283474.7:c.483A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.420A>G
  hgvsp: ENST00000591401.1:c.420A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.588A>G
  hgvsp: ENST00000590891.1:c.588A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-632A>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.408A>G
  hgvsp: ENST00000587615.1:c.408A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.303A>G
  hgvsp: ENST00000591897.1:c.303A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*299A>G
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9995
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3920
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3482
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln161Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

16-4659688-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659688
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659688
    reference: chr 16
allele count: 1
allele frequency: 1.022745868106693e-5
allele num: 97776
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*296C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.417C>A
  hgvsp: ENST00000591401.1:c.417C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.405C>A
  hgvsp: ENST00000587615.1:c.405C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.585C>A
  hgvsp: ENST00000590891.1:c.585C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-635C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.300C>A
  hgvsp: ENST00000591897.1:c.300C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.480C>A
  hgvsp: ENST00000283474.7:c.480C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10136
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3744
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3417
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro160Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

16-4659691-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659691
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659691
    reference: chr 16
allele count: 1
allele frequency: 1.022306732912143e-5
allele num: 97818
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.414C>A
  hgvsp: ENST00000591401.1:c.414C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*293C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.582C>A
  hgvsp: ENST00000590891.1:c.582C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.402C>A
  hgvsp: ENST00000587615.1:c.402C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-638C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.297C>A
  hgvsp: ENST00000591897.1:c.297C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.477C>A
  hgvsp: ENST00000283474.7:c.477C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3881
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3367
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 755
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40742
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3253
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala159Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

16-4659692-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659692
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659692
    reference: chr 16
allele count: 1
allele frequency: 1.022515797869077e-5
allele num: 97798
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*292C>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.581C>G
  hgvsp: ENSP00000465706.1:p.Ala194Gly
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.296C>G
  hgvsp: ENSP00000464725.1:p.Ala99Gly
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.413C>G
  hgvsp: ENSP00000467671.1:p.Ala138Gly
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.476C>G
  hgvsp: ENSP00000283474.6:p.Ala159Gly
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.401C>G
  hgvsp: ENSP00000466404.1:p.Ala134Gly
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-639C>G
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10237
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3718
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 535
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40799
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3382
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3281
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala159Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

16-4659712-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659712
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659712
    reference: chr 16
allele count: 1
allele frequency: 1.013048058999919e-5
allele num: 98712
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*272T>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.276T>A
  hgvsp: ENST00000591897.1:c.276T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-659T>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.393T>A
  hgvsp: ENST00000591401.1:c.393T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.381T>A
  hgvsp: ENST00000587615.1:c.381T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.561T>A
  hgvsp: ENST00000590891.1:c.561T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.456T>A
  hgvsp: ENST00000283474.7:c.456T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3374
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41761
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3457
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala152Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

16-4659715-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659715
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659715
    reference: chr 16
allele count: 5
allele frequency: 5.066677475578614e-5
allele num: 98684
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.453G>A
  hgvsp: ENST00000283474.7:c.453G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.273G>A
  hgvsp: ENST00000591897.1:c.273G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*269G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.558G>A
  hgvsp: ENST00000590891.1:c.558G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.390G>A
  hgvsp: ENST00000591401.1:c.390G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.378G>A
  hgvsp: ENST00000587615.1:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-662G>A
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3377
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10655
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3807
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1526
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2106
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34441
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 9.75e1
  variant carriers: 5
hgvs: p.Pro151Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/16-4659720-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659720
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659720
    reference: chr 16
allele count: 1
allele frequency: 1.013499817570033e-5
allele num: 98668
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.385T>G
  hgvsp: ENSP00000467671.1:p.Ser129Ala
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.553T>G
  hgvsp: ENSP00000465706.1:p.Ser185Ala
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.373T>G
  hgvsp: ENSP00000466404.1:p.Ser125Ala
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.448T>G
  hgvsp: ENSP00000283474.6:p.Ser150Ala
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*264T>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.268T>G
  hgvsp: ENSP00000464725.1:p.Ser90Ala
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-667T>G
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34197
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10609
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41552
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3568
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser150Ala
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

16-4659723-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659723
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659723
    reference: chr 16
allele count: 1
allele frequency: 1.014486872539869e-5
allele num: 98572
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.445C>T
  hgvsp: ENSP00000283474.6:p.Pro149Ser
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.550C>T
  hgvsp: ENSP00000465706.1:p.Pro184Ser
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.382C>T
  hgvsp: ENSP00000467671.1:p.Pro128Ser
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*261C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.370C>T
  hgvsp: ENSP00000466404.1:p.Pro124Ser
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-670C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.265C>T
  hgvsp: ENSP00000464725.1:p.Pro89Ser
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*261C>T
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3908
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3495
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33912
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2107
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41254
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro149Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

16-4659732-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659732
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659732
    reference: chr 16
allele count: 1
allele frequency: 1.020949891779311e-5
allele num: 97948
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.541C>A
  hgvsp: ENSP00000465706.1:p.Pro181Thr
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.436C>A
  hgvsp: ENSP00000283474.6:p.Pro146Thr
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.373C>A
  hgvsp: ENSP00000467671.1:p.Pro125Thr
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.361C>A
  hgvsp: ENSP00000466404.1:p.Pro121Thr
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.256C>A
  hgvsp: ENSP00000464725.1:p.Pro86Thr
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-679C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*252C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*252C>A
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2829
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32517
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 499
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3848
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5434
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro146Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/16-4659733-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659733
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659733
    reference: chr 16
allele count: 1
allele frequency: 1.020658120356006e-5
allele num: 97976
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.540T>G
  hgvsp: ENST00000590891.1:c.540T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.372T>G
  hgvsp: ENST00000591401.1:c.372T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*251T>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.360T>G
  hgvsp: ENST00000587615.1:c.360T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-680T>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*251T>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.255T>G
  hgvsp: ENST00000591897.1:c.255T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.435T>G
  hgvsp: ENST00000283474.7:c.435T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 748
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3694
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2839
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3889
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5474
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr145Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/16-4659745-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659745
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659745
    reference: chr 16
allele count: 4
allele frequency: 4.187429337129936e-5
allele num: 95524
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.360G>T
  hgvsp: ENST00000591401.1:c.360G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*239G>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.243G>T
  hgvsp: ENST00000591897.1:c.243G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.423G>T
  hgvsp: ENST00000283474.7:c.423G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.348G>T
  hgvsp: ENST00000587615.1:c.348G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.528G>T
  hgvsp: ENST00000590891.1:c.528G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*239G>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-692G>T
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4722
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1916
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4546
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7362
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1202
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro141Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD

16-4659745-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659745
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659745
    reference: chr 16
allele count: 1
allele frequency: 1.046857334282484e-5
allele num: 95524
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.423G>A
  hgvsp: ENST00000283474.7:c.423G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*239G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.528G>A
  hgvsp: ENST00000590891.1:c.528G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.360G>A
  hgvsp: ENST00000591401.1:c.360G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*239G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.243G>A
  hgvsp: ENST00000591897.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.348G>A
  hgvsp: ENST00000587615.1:c.348G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-692G>A
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4722
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5001
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2003
  bin: 3.25e1
  variant carriers: 0
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: 1916
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9684
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4337
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4546
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro141Pro
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-4659746-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659746
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659746
    reference: chr 16
allele count: 4
allele frequency: 4.230744822626023e-5
allele num: 94546
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.359C>T
  hgvsp: ENSP00000467671.1:p.Pro120Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-693C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.422C>T
  hgvsp: ENSP00000283474.6:p.Pro141Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.527C>T
  hgvsp: ENSP00000465706.1:p.Pro176Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*238C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.347C>T
  hgvsp: ENSP00000466404.1:p.Pro116Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*238C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.242C>T
  hgvsp: ENSP00000464725.1:p.Pro81Leu
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2333
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4803
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5828
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4683
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9357
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1445
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3218
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 640
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 804
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4615
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1403
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro141Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

16-4659755-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659755
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659755
    reference: chr 16
allele count: 1
allele frequency: 1.078050884001725e-5
allele num: 92760
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.233A>G
  hgvsp: ENSP00000464725.1:p.Gln78Arg
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-702A>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*229A>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.338A>G
  hgvsp: ENSP00000466404.1:p.Gln113Arg
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.518A>G
  hgvsp: ENSP00000465706.1:p.Gln173Arg
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.350A>G
  hgvsp: ENSP00000467671.1:p.Gln117Arg
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.413A>G
  hgvsp: ENSP00000283474.6:p.Gln138Arg
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*229A>G
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5186
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1801
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln138Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

16-4659757-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659757
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659757
    reference: chr 16
allele count: 1
allele frequency: 1.085658451851048e-5
allele num: 92110
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*227C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-704C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*227C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.348C>T
  hgvsp: ENST00000591401.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.336C>T
  hgvsp: ENST00000587615.1:c.336C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.231C>T
  hgvsp: ENST00000591897.1:c.231C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.516C>T
  hgvsp: ENST00000590891.1:c.516C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.411C>T
  hgvsp: ENST00000283474.7:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7742
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5465
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5295
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1135
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 478
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5326
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2038
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 506
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His137His
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-4659758-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659758
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659758
    reference: chr 16
allele count: 24
allele frequency: 2.755580049600441e-4
allele num: 87096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.515A>C
  hgvsp: ENSP00000465706.1:p.His172Pro
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.410A>C
  hgvsp: ENSP00000283474.6:p.His137Pro
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.230A>C
  hgvsp: ENSP00000464725.1:p.His77Pro
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*226A>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.335A>C
  hgvsp: ENSP00000466404.1:p.His112Pro
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.347A>C
  hgvsp: ENSP00000467671.1:p.His116Pro
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-705A>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*226A>C
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.95to100.00
genotype depth: GenotypeDepth
  all individuals: 5257
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8007
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 23846
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5487
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8514
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3376
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9177
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 664
  bin: 1.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 7.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 7.75e1
  variant carriers: 1
hgvs: p.His137Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

16-4659761-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659761
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659761
    reference: chr 16
allele count: 7
allele frequency: 7.787988696290692e-5
allele num: 89882
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.344A>C
  hgvsp: ENSP00000467671.1:p.His115Pro
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.407A>C
  hgvsp: ENSP00000283474.6:p.His136Pro
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*223A>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.332A>C
  hgvsp: ENSP00000466404.1:p.His111Pro
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.227A>C
  hgvsp: ENSP00000464725.1:p.His76Pro
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-708A>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.512A>C
  hgvsp: ENSP00000465706.1:p.His171Pro
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*223A>C
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8815
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5923
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3309
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5690
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1980
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10990
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1009
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2739
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27856
  bin: 6.25e1
  variant carriers: 0
hgvs: p.His136Pro
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

16-4659764-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659764
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659764
    reference: chr 16
allele count: 1
allele frequency: 1.120498397687291e-5
allele num: 89246
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.341A>G
  hgvsp: ENSP00000467671.1:p.Gln114Arg
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-711A>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*220A>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*220A>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.329A>G
  hgvsp: ENSP00000466404.1:p.Gln110Arg
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.404A>G
  hgvsp: ENSP00000283474.6:p.Gln135Arg
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.224A>G
  hgvsp: ENSP00000464725.1:p.Gln75Arg
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.509A>G
  hgvsp: ENSP00000465706.1:p.Gln170Arg
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21477
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5923
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5868
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1086
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2238
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gln135Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-4659769-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659769
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659769
    reference: chr 16
allele count: 1
allele frequency: 1.156416957698268e-5
allele num: 86474
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.399C>T
  hgvsp: ENST00000283474.7:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.336C>T
  hgvsp: ENST00000591401.1:c.336C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.219C>T
  hgvsp: ENST00000591897.1:c.219C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.324C>T
  hgvsp: ENST00000587615.1:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*215C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.504C>T
  hgvsp: ENST00000590891.1:c.504C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*215C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-716C>T
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4647
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6870
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2717
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13421
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5979
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1060
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly133Gly
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff

16-4659769-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659769
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659768
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 86474
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-717delG
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.335delG
  hgvsp: ENSP00000467671.1:p.Gly112AlafsTer91
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.218delG
  hgvsp: ENSP00000464725.1:p.Gly73AlafsTer91
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*214delG
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.398delG
  hgvsp: ENSP00000283474.6:p.Gly133AlafsTer91
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.323delG
  hgvsp: ENSP00000466404.1:p.Gly108AlafsTer91
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.503delG
  hgvsp: ENSP00000465706.1:p.Gly168AlafsTer91
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*214delG
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL96.00to97.00
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6870
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6111
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4647
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2255
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2925
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1448
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5979
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly133AlafsTer91
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: GC
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP

16-4659770-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659770
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659770
    reference: chr 16
allele count: 38
allele frequency: 4.405082073634424e-4
allele num: 86264
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.398G>A
  hgvsp: ENSP00000283474.6:p.Gly133Asp
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-717G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.503G>A
  hgvsp: ENSP00000465706.1:p.Gly168Asp
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.335G>A
  hgvsp: ENSP00000467671.1:p.Gly112Asp
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*214G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.323G>A
  hgvsp: ENSP00000466404.1:p.Gly108Asp
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.218G>A
  hgvsp: ENSP00000464725.1:p.Gly73Asp
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*214G>A
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7886
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6146
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18195
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6924
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11156
  bin: 1.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4629
  bin: 1.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2247
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1096
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2695
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 671
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly133Asp
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

16-4659771-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659771
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659771
    reference: chr 16
allele count: 1
allele frequency: 1.169590643274854e-5
allele num: 85500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-718G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*213G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.397G>A
  hgvsp: ENSP00000283474.6:p.Gly133Ser
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.217G>A
  hgvsp: ENSP00000464725.1:p.Gly73Ser
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.334G>A
  hgvsp: ENSP00000467671.1:p.Gly112Ser
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.322G>A
  hgvsp: ENSP00000466404.1:p.Gly108Ser
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*213G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.502G>A
  hgvsp: ENSP00000465706.1:p.Gly168Ser
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6284
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7384
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11906
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5065
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1579
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1597
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2144
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 867
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gly133Ser
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: QD

16-4659775-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659775
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659775
    reference: chr 16
allele count: 1
allele frequency: 1.196172248803828e-5
allele num: 83600
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-722G>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.330G>C
  hgvsp: ENST00000591401.1:c.330G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.213G>C
  hgvsp: ENST00000591897.1:c.213G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.318G>C
  hgvsp: ENST00000587615.1:c.318G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.498G>C
  hgvsp: ENST00000590891.1:c.498G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*209G>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*209G>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.393G>C
  hgvsp: ENST00000283474.7:c.393G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1657
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1345
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2027
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 392
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Pro131Pro
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

16-4659775-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659775
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659775
    reference: chr 16
allele count: 1
allele frequency: 1.196172248803828e-5
allele num: 83600
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*209G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.318G>A
  hgvsp: ENST00000587615.1:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.213G>A
  hgvsp: ENST00000591897.1:c.213G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-722G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.393G>A
  hgvsp: ENST00000283474.7:c.393G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.498G>A
  hgvsp: ENST00000590891.1:c.498G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.330G>A
  hgvsp: ENST00000591401.1:c.330G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*209G>A
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6521
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1477
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7220
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14617
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6422
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 858
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro131Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

16-4659776-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659776
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659776
    reference: chr 16
allele count: 16
allele frequency: 1.907941807774863e-4
allele num: 83860
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.317C>T
  hgvsp: ENSP00000466404.1:p.Pro106Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*208C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.497C>T
  hgvsp: ENSP00000465706.1:p.Pro166Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.212C>T
  hgvsp: ENSP00000464725.1:p.Pro71Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-723C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.329C>T
  hgvsp: ENSP00000467671.1:p.Pro110Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*208C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.392C>T
  hgvsp: ENSP00000283474.6:p.Pro131Leu
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7836
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7208
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12683
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6672
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5309
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15732
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 9.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1623
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15299
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro131Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

16-4659777-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659777
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659777
    reference: chr 16
allele count: 1
allele frequency: 1.189909566872918e-5
allele num: 84040
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.496C>G
  hgvsp: ENSP00000465706.1:p.Pro166Ala
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.211C>G
  hgvsp: ENSP00000464725.1:p.Pro71Ala
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-724C>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*207C>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.391C>G
  hgvsp: ENSP00000283474.6:p.Pro131Ala
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.316C>G
  hgvsp: ENSP00000466404.1:p.Pro106Ala
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*207C>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.328C>G
  hgvsp: ENSP00000467671.1:p.Pro110Ala
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15492
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6772
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12903
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7981
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7082
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3420
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 396
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6827
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 734
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2140
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro131Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: QD

16-4659779-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659779
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659779
    reference: chr 16
allele count: 1
allele frequency: 1.205661787755299e-5
allele num: 82942
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*205C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*205C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.326C>T
  hgvsp: ENSP00000467671.1:p.Pro109Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-726C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.494C>T
  hgvsp: ENSP00000465706.1:p.Pro165Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.209C>T
  hgvsp: ENSP00000464725.1:p.Pro70Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.389C>T
  hgvsp: ENSP00000283474.6:p.Pro130Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.314C>T
  hgvsp: ENSP00000466404.1:p.Pro105Leu
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6899
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13646
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1277
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14499
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6030
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6886
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3389
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16165
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro130Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

16-4659782-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659782
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659782
    reference: chr 16
allele count: 1
allele frequency: 1.229437655216504e-5
allele num: 81338
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.491C>T
  hgvsp: ENSP00000465706.1:p.Ser164Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.323C>T
  hgvsp: ENSP00000467671.1:p.Ser108Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*202C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.386C>T
  hgvsp: ENSP00000283474.6:p.Ser129Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*202C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-729C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.311C>T
  hgvsp: ENSP00000466404.1:p.Ser104Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.206C>T
  hgvsp: ENSP00000464725.1:p.Ser69Leu
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5953
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14053
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7098
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13736
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8880
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16359
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1726
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3868
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15069
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1225
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser129Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

16-4659788-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659788
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659788
    reference: chr 16
allele count: 4
allele frequency: 5.027904872039821e-5
allele num: 79556
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.485C>T
  hgvsp: ENSP00000465706.1:p.Ala162Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-735C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.380C>T
  hgvsp: ENSP00000283474.6:p.Ala127Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*196C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.317C>T
  hgvsp: ENSP00000467671.1:p.Ala106Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.200C>T
  hgvsp: ENSP00000464725.1:p.Ala67Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*196C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.305C>T
  hgvsp: ENSP00000466404.1:p.Ala102Val
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6128
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9737
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7381
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5750
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1354
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1052
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1046
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7433
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala127Val
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP

16-4659790-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659790
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659790
    reference: chr 16
allele count: 1
allele frequency: 1.26151129052605e-5
allele num: 79270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-737G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*194G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.303G>A
  hgvsp: ENST00000587615.1:c.303G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.378G>A
  hgvsp: ENST00000283474.7:c.378G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.315G>A
  hgvsp: ENST00000591401.1:c.315G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.198G>A
  hgvsp: ENST00000591897.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.483G>A
  hgvsp: ENST00000590891.1:c.483G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*194G>A
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7498
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10028
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14541
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5997
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13193
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3822
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 928
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1101
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 800
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr126Thr
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

16-4659791-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659791
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659791
    reference: chr 16
allele count: 17
allele frequency: 2.1424610576196e-4
allele num: 79348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.314C>T
  hgvsp: ENSP00000467671.1:p.Thr105Met
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.482C>T
  hgvsp: ENSP00000465706.1:p.Thr161Met
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.377C>T
  hgvsp: ENSP00000283474.6:p.Thr126Met
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*193C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.197C>T
  hgvsp: ENSP00000464725.1:p.Thr66Met
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-738C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.302C>T
  hgvsp: ENSP00000466404.1:p.Thr101Met
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*193C>T
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10195
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7527
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13347
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14559
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5655
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5705
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3752
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15647
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 927
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 7.75e1
  variant carriers: 1
hgvs: p.Thr126Met
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff

16-4659802-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659802
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659802
    reference: chr 16
allele count: 1
allele frequency: 1.28846054733804e-5
allele num: 77612
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.186C>T
  hgvsp: ENST00000591897.1:c.186C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.471C>T
  hgvsp: ENST00000590891.1:c.471C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-749C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*182C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.291C>T
  hgvsp: ENST00000587615.1:c.291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*182C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.366C>T
  hgvsp: ENST00000283474.7:c.366C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.303C>T
  hgvsp: ENST00000591401.1:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11453
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11456
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7618
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15932
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1245
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 745
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1791
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3770
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 876
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser122Ser
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ

16-4659805-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659805
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659805
    reference: chr 16
allele count: 3
allele frequency: 3.876069149073619e-5
allele num: 77398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.468C>T
  hgvsp: ENST00000590891.1:c.468C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.288C>T
  hgvsp: ENST00000587615.1:c.288C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.183C>T
  hgvsp: ENST00000591897.1:c.183C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.363C>T
  hgvsp: ENST00000283474.7:c.363C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.300C>T
  hgvsp: ENST00000591401.1:c.300C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-752C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*179C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*179C>T
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11421
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7628
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11746
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16070
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1765
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4139
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12899
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7684
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3782
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala121Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

16-4659808-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659808
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659808
    reference: chr 16
allele count: 6
allele frequency: 7.849909726038151e-5
allele num: 76434
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.360G>A
  hgvsp: ENST00000283474.7:c.360G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*176G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-755G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.180G>A
  hgvsp: ENST00000591897.1:c.180G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.465G>A
  hgvsp: ENST00000590891.1:c.465G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.297G>A
  hgvsp: ENST00000591401.1:c.297G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.285G>A
  hgvsp: ENST00000587615.1:c.285G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*176G>A
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16380
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12047
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7603
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6501
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10778
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 762
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4398
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4238
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7707
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21460
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 642
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala120Ala
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

16-4659809-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659809
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659809
    reference: chr 16
allele count: 9
allele frequency: 1.18994103181109e-4
allele num: 75634
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.359C>T
  hgvsp: ENSP00000283474.6:p.Ala120Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.296C>T
  hgvsp: ENSP00000467671.1:p.Ala99Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.464C>T
  hgvsp: ENSP00000465706.1:p.Ala155Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*175C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.284C>T
  hgvsp: ENSP00000466404.1:p.Ala95Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.179C>T
  hgvsp: ENSP00000464725.1:p.Ala60Val
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*175C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-756C>T
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4463
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16363
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6431
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7561
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10751
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12168
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3747
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7782
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1289
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1721
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala120Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/16-4659811-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659811
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659811
    reference: chr 16
allele count: 1
allele frequency: 1.30941469163284e-5
allele num: 76370
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*173T>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.294T>G
  hgvsp: ENST00000591401.1:c.294T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.282T>G
  hgvsp: ENST00000587615.1:c.282T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*173T>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.177T>G
  hgvsp: ENST00000591897.1:c.177T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.357T>G
  hgvsp: ENST00000283474.7:c.357T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.462T>G
  hgvsp: ENST00000590891.1:c.462T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-758T>G
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7556
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16716
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12478
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6391
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  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: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 521
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22568
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7753
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser119Ser
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

16-4659811-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659811
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659811
    reference: chr 16
allele count: 2
allele frequency: 2.61882938326568e-5
allele num: 76370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*173T>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-758T>C
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.357T>C
  hgvsp: ENST00000283474.7:c.357T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.462T>C
  hgvsp: ENST00000590891.1:c.462T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.294T>C
  hgvsp: ENST00000591401.1:c.294T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.177T>C
  hgvsp: ENST00000591897.1:c.177T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.282T>C
  hgvsp: ENST00000587615.1:c.282T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*173T>C
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16716
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6391
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12478
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10418
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 716
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7556
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4382
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 292
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1677
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3850
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7753
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser119Ser
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

16-4659812-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659812
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659812
    reference: chr 16
allele count: 1
allele frequency: 1.308660716622608e-5
allele num: 76414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*172C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.356C>T
  hgvsp: ENSP00000283474.6:p.Ser119Phe
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.176C>T
  hgvsp: ENSP00000464725.1:p.Ser59Phe
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.293C>T
  hgvsp: ENSP00000467671.1:p.Ser98Phe
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.461C>T
  hgvsp: ENSP00000465706.1:p.Ser154Phe
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*172C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.281C>T
  hgvsp: ENSP00000466404.1:p.Ser94Phe
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-759C>T
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10089
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12583
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7537
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16865
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6555
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1154
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 277
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ser119Phe
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ

16-4659825-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659825
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659825
    reference: chr 16
allele count: 30
allele frequency: 4.087416207967736e-4
allele num: 73396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-772G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.268G>A
  hgvsp: ENSP00000466404.1:p.Ala90Thr
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.280G>A
  hgvsp: ENSP00000467671.1:p.Ala94Thr
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*159G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.343G>A
  hgvsp: ENSP00000283474.6:p.Ala115Thr
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*159G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.163G>A
  hgvsp: ENSP00000464725.1:p.Ala55Thr
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.448G>A
  hgvsp: ENSP00000465706.1:p.Ala150Thr
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7565
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17590
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7748
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8257
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 13591
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3395
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 9.75e1
  variant carriers: 26
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1759
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8359
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23998
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala115Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

16-4659826-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659826
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659826
    reference: chr 16
allele count: 88
allele frequency: 1.194580946433904e-3
allele num: 73666
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.267C>T
  hgvsp: ENST00000587615.1:c.267C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.447C>T
  hgvsp: ENST00000590891.1:c.447C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.279C>T
  hgvsp: ENST00000591401.1:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.342C>T
  hgvsp: ENST00000283474.7:c.342C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-773C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.162C>T
  hgvsp: ENST00000591897.1:c.162C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*158C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*158C>T
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17633
  bin: 1.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 3356
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7566
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13730
  bin: 7.5e0
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 7603
  bin: 2.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8282
  bin: 1.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 4396
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 4.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1557
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7897
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 9.25e1
  variant carriers: 4
hgvs: p.Ala114Ala
num of homozygotes: 1
population: Latino
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum

16-4659827-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659827
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659827
    reference: chr 16
allele count: 1
allele frequency: 1.364479860277262e-5
allele num: 73288
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-774C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.446C>A
  hgvsp: ENSP00000465706.1:p.Ala149Asp
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*157C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.266C>A
  hgvsp: ENSP00000466404.1:p.Ala89Asp
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.278C>A
  hgvsp: ENSP00000467671.1:p.Ala93Asp
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*157C>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.341C>A
  hgvsp: ENSP00000283474.6:p.Ala114Asp
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.161C>A
  hgvsp: ENSP00000464725.1:p.Ala54Asp
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17736
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7593
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13749
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4888
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1188
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24530
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8543
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 882
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala114Asp
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

16-4659832-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659832
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659832
    reference: chr 16
allele count: 2
allele frequency: 2.770927429410624e-5
allele num: 72178
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465847
  ensembl transcript: ENST00000591113
  gene symbol: UBALD1
  hgvsc: ENST00000591113.1:c.156C>G
  hgvsp: ENST00000591113.1:c.156C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.261C>G
  hgvsp: ENST00000587615.1:c.261C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*152C>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.441C>G
  hgvsp: ENST00000590891.1:c.441C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.156C>G
  hgvsp: ENST00000591897.1:c.156C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.336C>G
  hgvsp: ENST00000283474.7:c.336C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.273C>G
  hgvsp: ENST00000591401.1:c.273C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*152C>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-779C>G
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7740
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14079
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6030
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18101
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5865
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1737
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro112Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

16-4659833-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659833
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659833
    reference: chr 16
allele count: 1
allele frequency: 1.378397750454871e-5
allele num: 72548
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.155C>G
  hgvsp: ENSP00000464725.1:p.Pro52Arg
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-780C>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.272C>G
  hgvsp: ENSP00000467671.1:p.Pro91Arg
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.335C>G
  hgvsp: ENSP00000283474.6:p.Pro112Arg
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.260C>G
  hgvsp: ENSP00000466404.1:p.Pro87Arg
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*151C>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.440C>G
  hgvsp: ENSP00000465706.1:p.Pro147Arg
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*151C>G
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465847
  ensembl transcript: ENST00000591113
  gene symbol: UBALD1
  hgvsc: ENST00000591113.1:c.155C>G
  hgvsp: ENSP00000465847.1:p.Pro52Arg
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7708
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9081
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1710
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1303
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro112Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum

16-4659835-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659835
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659835
    reference: chr 16
allele count: 1
allele frequency: 1.389969976648504e-5
allele num: 71944
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*149C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-782C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.270C>T
  hgvsp: ENST00000591401.1:c.270C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.438C>T
  hgvsp: ENST00000590891.1:c.438C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.258C>T
  hgvsp: ENST00000587615.1:c.258C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465847
  ensembl transcript: ENST00000591113
  gene symbol: UBALD1
  hgvsc: ENST00000591113.1:c.153C>T
  hgvsp: ENST00000591113.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.153C>T
  hgvsp: ENST00000591897.1:c.153C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.333C>T
  hgvsp: ENST00000283474.7:c.333C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*149C>T
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7717
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9351
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4834
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Phe111Phe
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: Latino
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum

16-4659842-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659842
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659842
    reference: chr 16
allele count: 3
allele frequency: 6.168016777005633e-5
allele num: 48638
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*142C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-789C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.431C>T
  hgvsp: ENSP00000465706.1:p.Pro144Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*142C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465847
  ensembl transcript: ENST00000591113
  gene symbol: UBALD1
  hgvsc: ENST00000591113.1:c.146C>T
  hgvsp: ENSP00000465847.1:p.Pro49Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.326C>T
  hgvsp: ENSP00000283474.6:p.Pro109Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.251C>T
  hgvsp: ENSP00000466404.1:p.Pro84Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.146C>T
  hgvsp: ENSP00000464725.1:p.Pro49Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.263C>T
  hgvsp: ENSP00000467671.1:p.Pro88Leu
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8336
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9709
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3879
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17390
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16284
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro109Leu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

16-4659844-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659844
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659844
    reference: chr 16
allele count: 1
allele frequency: 2.142336861048031e-5
allele num: 46678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.144G>A
  hgvsp: ENST00000591897.1:c.144G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.249G>A
  hgvsp: ENST00000587615.1:c.249G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-791G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465847
  ensembl transcript: ENST00000591113
  gene symbol: UBALD1
  hgvsc: ENST00000591113.1:c.144G>A
  hgvsp: ENST00000591113.1:c.144G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.261G>A
  hgvsp: ENST00000591401.1:c.261G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.324G>A
  hgvsp: ENST00000283474.7:c.324G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*140G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*140G>A
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.429G>A
  hgvsp: ENST00000590891.1:c.429G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9587
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14839
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8585
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17236
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3625
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3355
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1712
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5167
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro108Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

16-4659845-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 4659845
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 4659845
    reference: chr 16
allele count: 4
allele frequency: 7.767593599502873e-5
allele num: 51496
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465041
  ensembl transcript: ENST00000588691
  gene symbol: UBALD1
  hgvsc: ENST00000588691.1:c.34-792C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000467671
  ensembl transcript: ENST00000591401
  gene symbol: UBALD1
  hgvsc: ENST00000591401.1:c.260C>T
  hgvsp: ENSP00000467671.1:p.Pro87Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000283474
  ensembl transcript: ENST00000283474
  gene symbol: UBALD1
  hgvsc: ENST00000283474.7:c.323C>T
  hgvsp: ENSP00000283474.6:p.Pro108Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465745
  ensembl transcript: ENST00000587649
  gene symbol: UBALD1
  hgvsc: ENST00000587649.1:c.*139C>T
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465706
  ensembl transcript: ENST00000590891
  gene symbol: UBALD1
  hgvsc: ENST00000590891.1:c.428C>T
  hgvsp: ENSP00000465706.1:p.Pro143Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000465847
  ensembl transcript: ENST00000591113
  gene symbol: UBALD1
  hgvsc: ENST00000591113.1:c.143C>T
  hgvsp: ENSP00000465847.1:p.Pro48Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000464725
  ensembl transcript: ENST00000591897
  gene symbol: UBALD1
  hgvsc: ENST00000591897.1:c.143C>T
  hgvsp: ENSP00000464725.1:p.Pro48Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466404
  ensembl transcript: ENST00000587615
  gene symbol: UBALD1
  hgvsc: ENST00000587615.1:c.248C>T
  hgvsp: ENSP00000466404.1:p.Pro83Leu
  variant of: http://identifiers.org/hgnc/29576
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000153443
  ensembl protein: ENSP00000466361
  ensembl transcript: ENST00000590965
  gene symbol: UBALD1
  hgvsc: ENST00000590965.1:c.*139C>T
  variant of: http://identifiers.org/hgnc/29576
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17018
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9615
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8951
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14997
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1727
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3757
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro108Leu
num of homozygotes: 0
population: African
reference allele: G

GenotypeQuality
all individuals: 14584
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2008
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6525
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 68
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2375
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5914
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1810
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 883
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35328
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 6.765899864682003e-4
allele num: 4434
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5046
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 346
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4674
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2928
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.629999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.866e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.11371e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.57e-2

QD
type: SiteQuality
SIO_000300: 6.7e0

GenotypeQuality
all individuals: 8079
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1571
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6299
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15748
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4195
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.75e1
variant carriers: 4

South Asian
type: Population
allele count: 1
allele frequency: 1.967729240456513e-4
allele num: 5082
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.133105802047782e-4
allele num: 4688
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 4.260758414997869e-4
allele num: 4694
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2956
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35552
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.33051e5

ClippingRankSum
type: SiteQuality
SIO_000300: -5.09e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.57e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.824e0

QD
type: SiteQuality
SIO_000300: 1.126e1

MQRankSum
type: SiteQuality
SIO_000300: -4.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.57e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.66e-1

GenotypeQuality
all individuals: 404
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3901
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1107
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1261
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1355
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1012
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1244
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5118
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4486
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.093802345058626e-4
allele num: 4776
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2956
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.595970900951315e-5
allele num: 35740
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.140000000000001e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.58e-2

FS
type: SiteQuality
SIO_000300: 7.448e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e-1

DP
type: SiteQuality
SIO_000300: 6.44329e5

VQSLOD
type: SiteQuality
SIO_000300: -2.898e-1

GenotypeQuality
all individuals: 214
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1222
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16629
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10316
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 875
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5798
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1143
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1136
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3014
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4820
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5190
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.190100744634253e-4
allele num: 4566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36290
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4856
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 6.60132e5

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.37e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.164e0

VQSLOD
type: SiteQuality
SIO_000300: -4.596e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.408e1

GenotypeQuality
all individuals: 52
bin: 9.75e1
variant carriers: 25

GenotypeQuality
all individuals: 1051
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3124
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5605
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11590
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 993
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3060
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4632
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4882
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 24
allele frequency: 6.506180871828237e-4
allele num: 36888
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 378
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4922
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.33e-2

DP
type: SiteQuality
SIO_000300: 6.84078e5

FS
type: SiteQuality
SIO_000300: 6.742e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.67e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

QD
type: SiteQuality
SIO_000300: 1.387e1

GenotypeQuality
all individuals: 719
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 4941
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 4.25e1
variant carriers: 3

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 3

GenotypeQuality
all individuals: 15294
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 282
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 94
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2394
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 7.25e1
variant carriers: 1

African
type: Population
allele count: 2
allele frequency: 4.156275976724855e-4
allele num: 4812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5044
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 1.583280557314756e-3
allele num: 3158
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5442
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 2.512562814070352e-3
allele num: 398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 191
allele frequency: 4.993464052287582e-3
allele num: 38250
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 3.78931413414172e-4
allele num: 5278
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.1e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.39131e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.07e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.403e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

GenotypeQuality
all individuals: 729
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1027
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 105
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 747
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15508
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5436
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5112
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.285479226655697e-4
allele num: 38896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3226
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4872
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.564e0

MQRankSum
type: SiteQuality
SIO_000300: -4.6e-2

VQSLOD
type: SiteQuality
SIO_000300: 8.5e-1

DP
type: SiteQuality
SIO_000300: 7.54126e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.35e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.12e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.53e-1

QD
type: SiteQuality
SIO_000300: 1.405e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 4658
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4113
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 645
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3549
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1683
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.535496957403651e-5
allele num: 39440
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5592
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5182
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3280
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4916
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.06e-2

DP
type: SiteQuality
SIO_000300: 7.63821e5

VQSLOD
type: SiteQuality
SIO_000300: -6.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.632e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.55e-1

QD
type: SiteQuality
SIO_000300: 7.28e0

GenotypeQuality
all individuals: 884
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3688
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 708
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18463
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1765
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4968
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 40108
num of homozygotes: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 5.302226935312832e-4
allele num: 5658
num of homozygotes: 0

ClippingRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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SIO_000300: -5.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.62e0

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-2

QD
type: SiteQuality
SIO_000300: 1.023e1

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

African
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 5750
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 3.010234798314269e-4
allele num: 3322
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 416
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.493268175925002e-5
allele num: 40108
num of homozygotes: 0

South Asian
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num of homozygotes: 0

InbreedingCoeff
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VQSLOD
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MQ
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ReadPosRankSum
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MQRankSum
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QD
type: SiteQuality
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FS
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DP
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -9.22e-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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Other
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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allele num: 5064
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Latino
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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ClippingRankSum
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QD
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VQSLOD
type: SiteQuality
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MQRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
type: SiteQuality
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DP
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SIO_000300: 8.00272e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.01e-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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East Asian
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allele frequency: 1.874062968515742e-4
allele num: 5336
num of homozygotes: 0

South Asian
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European (Non-Finnish)
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allele frequency: 2.463539613716988e-5
allele num: 40592
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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African
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Other
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BaseQRankSum
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SIO_000300: -1.482e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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QD
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MQRankSum
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MQ
type: SiteQuality
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ReadPosRankSum
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DP
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SIO_000300: 8.00272e5

InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e-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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African
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allele frequency: 0.0e0
allele num: 5124
num of homozygotes: 0

East Asian
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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: 4.866416857267994e-5
allele num: 41098
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Latino
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num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.11388e5

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.813e0

MQRankSum
type: SiteQuality
SIO_000300: 4.67e-1

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.192e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-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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GenotypeQuality
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African
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allele frequency: 0.0e0
allele num: 5124
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 426
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South Asian
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allele frequency: 0.0e0
allele num: 5792
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European (Finnish)
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allele frequency: 0.0e0
allele num: 3390
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.433208428633997e-5
allele num: 41098
num of homozygotes: 0

East Asian
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allele frequency: 3.711952487008166e-4
allele num: 5388
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Latino
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allele frequency: 1.662786830728301e-4
allele num: 6014
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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 (Non-Finnish)
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allele frequency: 2.433208428633997e-5
allele num: 41098
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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East Asian
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African
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Latino
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allele num: 6014
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South Asian
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ClippingRankSum
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QD
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FS
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MQRankSum
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MQ
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VQSLOD
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BaseQRankSum
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DP
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InbreedingCoeff
type: SiteQuality
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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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South Asian
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African
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European (Finnish)
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European (Non-Finnish)
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Latino
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East Asian
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Other
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MQRankSum
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MQ
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QD
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BaseQRankSum
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DP
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InbreedingCoeff
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FS
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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European (Finnish)
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South Asian
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Other
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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MQ
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DP
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BaseQRankSum
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FS
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MQRankSum
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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Other
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South Asian
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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MQ
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FS
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QD
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VQSLOD
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ClippingRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4944
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.626617652575116e-5
allele num: 53318
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7976
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10010
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.313e0

VQSLOD
type: SiteQuality
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BaseQRankSum
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SIO_000300: 1.14e0

MQ
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QD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

MQRankSum
type: SiteQuality
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DP
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SIO_000300: 1.082365e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -5.45e-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
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 3
allele frequency: 6.142506142506142e-4
allele num: 4884
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7792
num of homozygotes: 0

European (Non-Finnish)
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allele count: 12
allele frequency: 2.231146809460062e-4
allele num: 53784
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10412
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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DP
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VQSLOD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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FS
type: SiteQuality
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InbreedingCoeff
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SIO_000300: -6.5e-3

BaseQRankSum
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QD
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MQ
type: SiteQuality
SIO_000300: 5.878e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
allele num: 8496
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10734
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7944
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.802841277853898e-5
allele num: 55468
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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QD
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MQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.4e-2

BaseQRankSum
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VQSLOD
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FS
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DP
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MQ
type: SiteQuality
SIO_000300: 5.906e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.3e-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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GenotypeQuality
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GenotypeQuality
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Other
type: Population
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allele frequency: 0.0e0
allele num: 650
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 7348
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 8024
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Latino
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allele frequency: 9.177679882525697e-5
allele num: 10896
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DP
type: SiteQuality
SIO_000300: 1.149586e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.014e0

MQRankSum
type: SiteQuality
SIO_000300: 2.46e-1

BaseQRankSum
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SIO_000300: -1.756e0

QD
type: SiteQuality
SIO_000300: 9.27e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.2e-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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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8658
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8026
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7354
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Latino
type: Population
allele count: 1
allele frequency: 9.1726288754357e-5
allele num: 10902
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56150
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5492
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.911e1

VQSLOD
type: SiteQuality
SIO_000300: 2.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.2e-2

DP
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QD
type: SiteQuality
SIO_000300: 1.364e1

FS
type: SiteQuality
SIO_000300: 5.256e0

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.21e-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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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.82882223847842e-4
allele num: 10936
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8676
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African
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allele count: 54
allele frequency: 7.303218826075196e-3
allele num: 7394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8048
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56330
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5534
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
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MQRankSum
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QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.156415e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.11e-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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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 56378
num of homozygotes: 0

African
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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: 2.305741295826608e-4
allele num: 8674
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Latino
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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MQ
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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ClippingRankSum
type: SiteQuality
SIO_000300: 4.64e-1

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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European (Non-Finnish)
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allele count: 1
allele frequency: 1.771165426850868e-5
allele num: 56460
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 9.127418765972983e-5
allele num: 10956
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8062
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 652
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.538e0

FS
type: SiteQuality
SIO_000300: 1.039e0

MQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

QD
type: SiteQuality
SIO_000300: 1.025e1

DP
type: SiteQuality
SIO_000300: 1.158751e6

GenotypeQuality
all individuals: 354
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4012
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 733
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3911
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 124
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10982
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.752049898381106e-5
allele num: 57076
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8694
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8092
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.26e-1

QD
type: SiteQuality
SIO_000300: 1.144e1

FS
type: SiteQuality
SIO_000300: 5.833e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.73e-1

DP
type: SiteQuality
SIO_000300: 1.169238e6

VQSLOD
type: SiteQuality
SIO_000300: 7.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.544e0

MQ
type: SiteQuality
SIO_000300: 5.924e1

GenotypeQuality
all individuals: 36
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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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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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.257992148065059e-5
allele num: 57056
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.237623762376238e-4
allele num: 8080
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.151012891344383e-4
allele num: 8688
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10980
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7624
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5590
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

QD
type: SiteQuality
SIO_000300: 8.57e0

FS
type: SiteQuality
SIO_000300: 3.042e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.04e-1

DP
type: SiteQuality
SIO_000300: 1.169506e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.37e-1

GenotypeQuality
all individuals: 117
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 45
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variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10960
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8072
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7638
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.75297128633033e-5
allele num: 57046
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8688
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.11e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.87e-1

QD
type: SiteQuality
SIO_000300: 1.303e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.4e-3

DP
type: SiteQuality
SIO_000300: 1.166298e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.15e-1

FS
type: SiteQuality
SIO_000300: 5.5e0

VQSLOD
type: SiteQuality
SIO_000300: -1.448e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

GenotypeQuality
all individuals: 4579
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 109
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variant carriers: 0

GenotypeQuality
all individuals: 3641
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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: 101
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variant carriers: 0

GenotypeQuality
all individuals: 320
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3875
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.753893643889434e-5
allele num: 57016
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10942
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7630
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8058
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8670
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.539999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-3

DP
type: SiteQuality
SIO_000300: 1.16439e6

VQSLOD
type: SiteQuality
SIO_000300: 1.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.32e-1

FS
type: SiteQuality
SIO_000300: 4.055e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.2e-1

MQ
type: SiteQuality
SIO_000300: 5.998e1

GenotypeQuality
all individuals: 141
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3739
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 39709
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variant carriers: 0

GenotypeQuality
all individuals: 382
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 172
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GenotypeQuality
all individuals: 600
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 673
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variant carriers: 0

GenotypeQuality
all individuals: 458
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variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10774
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.760439405675657e-5
allele num: 56804
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7994
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.08e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.972e0

DP
type: SiteQuality
SIO_000300: 1.148903e6

FS
type: SiteQuality
SIO_000300: 4.593e0

MQ
type: SiteQuality
SIO_000300: 5.794e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.697e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.0e-3

QD
type: SiteQuality
SIO_000300: 9.529999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.057e0

GenotypeQuality
all individuals: 169
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7992
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10780
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.759757857318833e-5
allele num: 56826
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7578
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5522
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.086e1

MQRankSum
type: SiteQuality
SIO_000300: -1.557e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.625e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.79e-1

FS
type: SiteQuality
SIO_000300: 9.86e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.169e0

MQ
type: SiteQuality
SIO_000300: 5.855e1

DP
type: SiteQuality
SIO_000300: 1.14911e6

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7816
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 640
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.208506037123806e-5
allele num: 55490
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5312
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.098966e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

QD
type: SiteQuality
SIO_000300: 9.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.12e-1

MQ
type: SiteQuality
SIO_000300: 5.92e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.98e-1

FS
type: SiteQuality
SIO_000300: 3.94e0

VQSLOD
type: SiteQuality
SIO_000300: 3.6e-2

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7362
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8470
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.802126509280952e-5
allele num: 55490
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7816
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5312
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.24e0

VQSLOD
type: SiteQuality
SIO_000300: 3.6e-2

FS
type: SiteQuality
SIO_000300: 3.94e0

MQ
type: SiteQuality
SIO_000300: 5.92e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-1

DP
type: SiteQuality
SIO_000300: 1.098966e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.98e-1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 8071
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GenotypeQuality
all individuals: 47
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variant carriers: 5

GenotypeQuality
all individuals: 151
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.639275056408763e-5
allele num: 54956
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8414
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.74649821477616e-4
allele num: 7282
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7738
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5264
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

DP
type: SiteQuality
SIO_000300: 1.079692e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.7e-3

FS
type: SiteQuality
SIO_000300: 2.689e0

QD
type: SiteQuality
SIO_000300: 1.072e1

GenotypeQuality
all individuals: 9328
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1807
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 30386
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2968
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8296
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7556
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10000
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5166
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.851783267286397e-5
allele num: 54002
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.371e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.28e-1

DP
type: SiteQuality
SIO_000300: 1.047637e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.996e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

MQRankSum
type: SiteQuality
SIO_000300: -7.9e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.33e-1

GenotypeQuality
all individuals: 552
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1989
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2911
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9914
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29105
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 451
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5092
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7060
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.8627524029506e-5
allele num: 53684
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8268
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

QD
type: SiteQuality
SIO_000300: 1.157e1

DP
type: SiteQuality
SIO_000300: 1.032405e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.91e0

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.15e-1

GenotypeQuality
all individuals: 1039
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2479
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1758
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 567
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3270
bin: 2.5e0
variant carriers: 1

GenotypeQuality
all individuals: 5086
bin: 7.5e0
variant carriers: 2

GenotypeQuality
all individuals: 735
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1918
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 27277
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 779
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 26
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 12
allele frequency: 2.364625206904706e-4
allele num: 50748
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 1.228878648233487e-3
allele num: 6510
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.321262766945218e-4
allele num: 4308
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.226391954868776e-4
allele num: 8154
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.046243984097091e-4
allele num: 9558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 562
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.378169790518192e-4
allele num: 7256
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.335e0

VQSLOD
type: SiteQuality
SIO_000300: -4.028e2

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.96789e2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.98e-2

DP
type: SiteQuality
SIO_000300: 1.040021e6

MQ
type: SiteQuality
SIO_000300: 5.845e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.03e0

QD
type: SiteQuality
SIO_000300: 1.07e0

GenotypeQuality
all individuals: 408
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5480
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 506
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2221
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 451
bin: 5.25e1
variant carriers: 1

African
type: Population
allele count: 3
allele frequency: 4.385964912280702e-4
allele num: 6840
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4792
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9706
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.636210912145394e-5
allele num: 52382
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8182
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.95e-1

DP
type: SiteQuality
SIO_000300: 1.006402e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-2

FS
type: SiteQuality
SIO_000300: 1.85656e2

MQ
type: SiteQuality
SIO_000300: 5.836e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.54e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.574e2

QD
type: SiteQuality
SIO_000300: 3.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.1e0

GenotypeQuality
all individuals: 663
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 416
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2478
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12109
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 480
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variant carriers: 0

GenotypeQuality
all individuals: 2680
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26345
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.918354818907305e-5
allele num: 52128
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8120
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6756
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7314
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4804
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.87578e5

MQRankSum
type: SiteQuality
SIO_000300: 4.75e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.1e-2

QD
type: SiteQuality
SIO_000300: 6.7e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.900000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.506e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.9e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

GenotypeQuality
all individuals: 2925
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1448
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
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variant carriers: 0

GenotypeQuality
all individuals: 22177
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2255
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9148
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.259128682951398e-4
allele num: 7942
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50644
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7060
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4602
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.379999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.044e0

DP
type: SiteQuality
SIO_000300: 9.51318e5

FS
type: SiteQuality
SIO_000300: 2.447e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 6.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.81e-2

GenotypeQuality
all individuals: 1060
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2717
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22177
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13421
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 609
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 881
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9148
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7942
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50644
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7060
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.81e-2

QD
type: SiteQuality
SIO_000300: 6.42e0

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.379999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.044e0

FS
type: SiteQuality
SIO_000300: 2.447e0

DP
type: SiteQuality
SIO_000300: 9.51318e5

GenotypeQuality
all individuals: 680
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6040
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13646
bin: 2.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2904
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22507
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 65
bin: 9.75e1
variant carriers: 32

GenotypeQuality
all individuals: 23
bin: 9.25e1
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GenotypeQuality
all individuals: 640
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1416
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 100
bin: 8.25e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7916
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.102292768959436e-4
allele num: 9072
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7056
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.91295746785361e-5
allele num: 50550
num of homozygotes: 0

African
type: Population
allele count: 33
allele frequency: 5.072241008300031e-3
allele num: 6506
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4596
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 568
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.25e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.3e-2

DP
type: SiteQuality
SIO_000300: 9.51318e5

QD
type: SiteQuality
SIO_000300: 1.26e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.75e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.303e0

GenotypeQuality
all individuals: 694
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14161
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 738
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1052
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2925
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20382
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6098
bin: 7.5e0
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GenotypeQuality
all individuals: 3167
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7900
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.112099644128114e-4
allele num: 8992
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50080
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6414
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6994
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.758e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.23e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.061e0

VQSLOD
type: SiteQuality
SIO_000300: -3.278e0

DP
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SIO_000300: 9.29912e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.54e-1

QD
type: SiteQuality
SIO_000300: 2.15e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4364
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.462843768285547e-4
allele num: 6836
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8726
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7792
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49082
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.83e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 9.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.69e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.939e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-2

DP
type: SiteQuality
SIO_000300: 9.13565e5

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49082
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 1.283367556468173e-4
allele num: 7792
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6836
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8726
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.939e1

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

FS
type: SiteQuality
SIO_000300: 9.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-2

DP
type: SiteQuality
SIO_000300: 9.13565e5

BaseQRankSum
type: SiteQuality
SIO_000300: 5.69e-1

GenotypeQuality
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variant carriers: 1

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.268602540834846e-4
allele num: 4408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8734
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7796
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6286
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6838
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 15
allele frequency: 3.044572542015101e-4
allele num: 49268
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.08979e5

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

MQRankSum
type: SiteQuality
SIO_000300: -3.87e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.2e-2

QD
type: SiteQuality
SIO_000300: 1.243e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.38e-2

FS
type: SiteQuality
SIO_000300: 7.05e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.717e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.47e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7822
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6856
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.026753141467369e-5
allele num: 49340
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8736
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 542
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.256e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.56e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.1e-2

MQ
type: SiteQuality
SIO_000300: 5.911e1

FS
type: SiteQuality
SIO_000300: 4.586e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.33e-2

DP
type: SiteQuality
SIO_000300: 9.01738e5

QD
type: SiteQuality
SIO_000300: 1.377e1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6196
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4362
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.052713687494868e-5
allele num: 48716
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7730
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6750
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 536
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.53e-1

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.32e-2

QD
type: SiteQuality
SIO_000300: 1.032e1

DP
type: SiteQuality
SIO_000300: 8.7507e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

ClippingRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47870
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6630
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8364
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6106
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South Asian
type: Population
allele count: 1
allele frequency: 1.309929263819754e-4
allele num: 7634
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4224
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.69e-1

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
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DP
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FS
type: SiteQuality
SIO_000300: 2.017e0

ReadPosRankSum
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MQ
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
type: Population
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allele frequency: 1.242236024844721e-4
allele num: 8050
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

South Asian
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allele frequency: 1.327668613913967e-4
allele num: 7532
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4058
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European (Non-Finnish)
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allele count: 2
allele frequency: 4.254232961796988e-5
allele num: 47012
num of homozygotes: 0

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

Latino
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num of homozygotes: 0

African
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.137939881130542e-5
allele num: 46774
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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East Asian
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allele count: 0
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.61e-2

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
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ReadPosRankSum
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DP
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ClippingRankSum
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QD
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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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.334044823906083e-4
allele num: 7496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5974
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 3.415008964398531e-4
allele num: 46852
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8018
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4066
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 514
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.317e1

MQRankSum
type: SiteQuality
SIO_000300: 3.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.294e0

FS
type: SiteQuality
SIO_000300: 4.265e0

DP
type: SiteQuality
SIO_000300: 8.43373e5

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 9.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.67e-2

GenotypeQuality
all individuals: 800
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1455
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7752
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.178459393516905e-5
allele num: 45904
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7378
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3940
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6254
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 7.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.64e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.26e0

DP
type: SiteQuality
SIO_000300: 8.10688e5

QD
type: SiteQuality
SIO_000300: 1.387e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 313
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3938
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 5.124701059104886e-4
allele num: 5854
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7374
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45772
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7682
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.632e0

VQSLOD
type: SiteQuality
SIO_000300: 2.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.2e0

MQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

DP
type: SiteQuality
SIO_000300: 8.05763e5

QD
type: SiteQuality
SIO_000300: 1.055e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.63e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 9.56e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQ
type: SiteQuality
SIO_000300: 5.934e1

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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GenotypeQuality
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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

GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7274
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.722356183258698e-4
allele num: 5806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.633645851760127e-5
allele num: 45224
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3850
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.639915522703273e-4
allele num: 7576
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6196
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.746e0

VQSLOD
type: SiteQuality
SIO_000300: 3.5e-1

DP
type: SiteQuality
SIO_000300: 7.97138e5

MQ
type: SiteQuality
SIO_000300: 5.913e1

MQRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.77e-2

QD
type: SiteQuality
SIO_000300: 1.27e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.169999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 1363
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 8

GenotypeQuality
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GenotypeQuality
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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: 703
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variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 2.024291497975709e-3
allele num: 494
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3830
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5752
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 5.550929780738274e-4
allele num: 7206
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7408
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 4.906771344455348e-4
allele num: 6114
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.230649118893598e-5
allele num: 44830
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.39e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.84e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.89e-1

QD
type: SiteQuality
SIO_000300: 1.234e1

DP
type: SiteQuality
SIO_000300: 7.98932e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -8.2e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.64e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 196
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GenotypeQuality
all individuals: 31
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6208
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7264
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.211997876482038e-5
allele num: 45208
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5812
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3838
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7530
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.25e0

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.68e-2

QD
type: SiteQuality
SIO_000300: 1.206e1

FS
type: SiteQuality
SIO_000300: 2.087e0

DP
type: SiteQuality
SIO_000300: 7.92307e5

ClippingRankSum
type: SiteQuality
SIO_000300: -7.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.01e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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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
all individuals: 31
bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 2
allele frequency: 3.441156228492773e-4
allele num: 5812
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3838
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45208
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7530
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.087e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.68e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.25e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.44e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.41e-1

QD
type: SiteQuality
SIO_000300: 1.206e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.01e0

DP
type: SiteQuality
SIO_000300: 7.92307e5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 492
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3820
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.613944480309877e-4
allele num: 6196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5814
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45258
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7262
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.461e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

VQSLOD
type: SiteQuality
SIO_000300: 4.13e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.8e-1

DP
type: SiteQuality
SIO_000300: 7.89011e5

QD
type: SiteQuality
SIO_000300: 1.094e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1011
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

African
type: Population
allele count: 26
allele frequency: 4.629629629629629e-3
allele num: 5616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.896868821555014e-5
allele num: 43498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 466
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.408847562693716e-4
allele num: 7098
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7162
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5954
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.94e0

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.72e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.56047e5

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.91e-2

QD
type: SiteQuality
SIO_000300: 1.259e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

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
all individuals: 1185
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GenotypeQuality
all individuals: 24328
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GenotypeQuality
all individuals: 1729
bin: 3.75e1
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GenotypeQuality
all individuals: 807
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GenotypeQuality
all individuals: 349
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GenotypeQuality
all individuals: 26
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 111
bin: 9.75e1
variant carriers: 83

GenotypeQuality
all individuals: 273
bin: 7.25e1
variant carriers: 2

Latino
type: Population
allele count: 8
allele frequency: 1.112966054535337e-3
allele num: 7188
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 4.201680672268907e-3
allele num: 476
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.402918069584736e-4
allele num: 7128
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.57653791130186e-4
allele num: 5592
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.771618625277162e-4
allele num: 3608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6002
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 74
allele frequency: 1.69444953288148e-3
allele num: 43672
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.54119e5

ClippingRankSum
type: SiteQuality
SIO_000300: -2.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.26e-1

FS
type: SiteQuality
SIO_000300: 1.742e0

VQSLOD
type: SiteQuality
SIO_000300: 3.89e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

QD
type: SiteQuality
SIO_000300: 1.314e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.72e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.01e-1

GenotypeQuality
all individuals: 199
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1724
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7801
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 70
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1500
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4354
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7124
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5956
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.794043774668102e-4
allele num: 5574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3564
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7102
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.743e0

DP
type: SiteQuality
SIO_000300: 7.5308e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.868e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.96e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.67e-1

QD
type: SiteQuality
SIO_000300: 6.05e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.557e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e0

GenotypeQuality
all individuals: 177
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9676
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1140
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5328
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 461
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24890
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1580
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4682
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3402
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.668098216786481e-5
allele num: 42844
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5928
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7076
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7032
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.33009e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.14e-2

FS
type: SiteQuality
SIO_000300: 1.7658e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.5e0

MQ
type: SiteQuality
SIO_000300: 5.884e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 9.890000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6162
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25339
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9682
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4671
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1111
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1067
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5339
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43102
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.406469760900141e-4
allele num: 7110
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5444
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5938
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7064
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3418
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

QD
type: SiteQuality
SIO_000300: 2.025e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.09e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.647e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: -1.766e0

DP
type: SiteQuality
SIO_000300: 7.33117e5

FS
type: SiteQuality
SIO_000300: 1.356e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e-1

GenotypeQuality
all individuals: 243
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1231
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1757
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5472
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1050
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10026
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 289
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5389
bin: 6.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42738
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.689760054072322e-4
allele num: 5918
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 472
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5384
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6982
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7070
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.69e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.108e1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.18e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

DP
type: SiteQuality
SIO_000300: 7.2623e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.52e0

GenotypeQuality
all individuals: 15313
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5098
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5662
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3500
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1729
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 240
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2851
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3717
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1708
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4032
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 5.344735435595938e-4
allele num: 3742
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.742767514813524e-4
allele num: 5738
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 29550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 306
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.156e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e0

DP
type: SiteQuality
SIO_000300: 6.5499e5

FS
type: SiteQuality
SIO_000300: 3.557e0

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

VQSLOD
type: SiteQuality
SIO_000300: -9.056999999999999e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.47e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.713e0

QD
type: SiteQuality
SIO_000300: 1.436e1

GenotypeQuality
all individuals: 5802
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15664
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15455
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3431
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 557
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 9.75e1
variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.525595825694543e-5
allele num: 28364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3358
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3596
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1642
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5518
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.97e-2

FS
type: SiteQuality
SIO_000300: 4.242e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -3.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.152e0

DP
type: SiteQuality
SIO_000300: 6.4962e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

QD
type: SiteQuality
SIO_000300: 1.052e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.71e-2

GenotypeQuality
all individuals: 538
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4762
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16441
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3533
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 806
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2051
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3744
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 18487
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4008
num of homozygotes: 0