X-15288042-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015288042
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015288042
    reference: chr 0
allele count: 1
allele frequency: 1.229755155748491e-5
allele num: 81317
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102048
  ensembl transcript: ENST00000473862
  gene symbol: ASB9
  hgvsc: ENST00000473862.1:n.94G>A
  variant of: http://identifiers.org/hgnc/17184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102048
  ensembl protein: ENSP00000369852
  ensembl transcript: ENST00000380485
  gene symbol: ASB9
  hgvsc: ENST00000380485.3:c.-46G>A
  variant of: http://identifiers.org/hgnc/17184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102048
  ensembl protein: ENSP00000369850
  ensembl transcript: ENST00000380483
  gene symbol: ASB9
  hgvsc: ENST00000380483.3:c.-46G>A
  variant of: http://identifiers.org/hgnc/17184
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102048
  ensembl protein: ENSP00000369855
  ensembl transcript: ENST00000380488
  gene symbol: ASB9
  hgvsc: ENST00000380488.4:c.-46G>A
  variant of: http://identifiers.org/hgnc/17184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000102048
  ensembl transcript: ENST00000470015
  gene symbol: ASB9
  hgvsc: ENST00000470015.1:n.131G>A
  variant of: http://identifiers.org/hgnc/17184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000102048
  ensembl protein: ENSP00000438943
  ensembl transcript: ENST00000546332
  gene symbol: ASB9
  hgvsc: ENST00000546332.1:c.-46G>A
  variant of: http://identifiers.org/hgnc/17184
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
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  bin: 9.25e1
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genotype quality: GenotypeQuality
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  bin: 2.75e1
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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
  all individuals: 4912
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10478
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

X-15301579-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301579
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301579
    reference: chr 0
allele count: 2
allele frequency: 2.281099946394151e-5
allele num: 87677
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.*48T>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.*48T>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.*48T>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.*48T>C
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

X-15301587-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301587
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301587
    reference: chr 0
allele count: 1
allele frequency: 1.140523956705711e-5
allele num: 87679
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.*40T>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.*40T>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.*40T>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.*40T>C
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15886
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 4.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: A
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff

X-15301595-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301595
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301595
    reference: chr 0
allele count: 1
allele frequency: 1.140523956705711e-5
allele num: 87679
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.*32G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.*32G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.*32G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.*32G>A
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 75
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  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

X-15301601-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301601
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301601
    reference: chr 0
allele count: 1
allele frequency: 1.140211851361983e-5
allele num: 87703
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.*26T>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.*26T>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.*26T>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.*26T>C
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12092
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6163
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3596
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2099
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17305
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7537
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2549
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3323
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23412
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-15301604-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301604
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301604
    reference: chr 0
allele count: 1
allele frequency: 1.140146850914398e-5
allele num: 87708
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.*23A>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.*23A>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.*23A>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.*23A>G
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12102
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 5.25e1
  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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  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23488
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3322
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7546
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1379
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2554
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

X-15301620-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301620
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301620
    reference: chr 0
allele count: 3
allele frequency: 3.41899823351758e-5
allele num: 87745
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.*7G>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.*7G>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.*7G>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.*7G>C
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4427
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  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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  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17308
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1383
  bin: 8.75e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23728
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2557
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum

X-15301624-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301624
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301624
    reference: chr 0
allele count: 4582
allele frequency: 5.22183094578732e-2
allele num: 87747
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.*3C>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.*3C>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.*3C>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.*3C>G
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4129
  bin: 9.75e1
  variant carriers: 3715
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
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  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 16269
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 5.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 8.25e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 3587
  bin: 4.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 5106
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12116
  bin: 3.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 7.25e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 6148
  bin: 3.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 6.75e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 5.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 9.25e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4399
  bin: 4.25e1
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 6.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 8.75e1
  variant carriers: 94
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
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  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2603
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  variant carriers: 6
genotype quality: GenotypeQuality
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
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genotype quality: GenotypeQuality
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  bin: 4.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2079
  bin: 9.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 8.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3300
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 23639
  bin: 6.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 2538
  bin: 7.25e1
  variant carriers: 5
num of homozygotes: 106
population: Other
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

X-15301628-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301628
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301628
    reference: chr 0
allele count: 3
allele frequency: 3.418647583016159e-5
allele num: 87754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.908A>G
  hgvsp: ENSP00000445465.1:p.Ter303TrpextTer2
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: stop_lost
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.971A>G
  hgvsp: ENSP00000417914.1:p.Ter324TrpextTer2
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*414A>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.920A>G
  hgvsp: ENSP00000369837.3:p.Ter307TrpextTer2
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.908A>G
  hgvsp: ENSP00000343408.4:p.Ter303TrpextTer2
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6626
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17418
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8076
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1484
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ter324TrpextTer2
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS

X-15301629-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301629
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301629
    reference: chr 0
allele count: 3
allele frequency: 3.418647583016159e-5
allele num: 87754
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*413T>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.907T>C
  hgvsp: ENSP00000445465.1:p.Ter303GlnextTer2
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.919T>C
  hgvsp: ENSP00000369837.3:p.Ter307GlnextTer2
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: stop_lost
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.907T>C
  hgvsp: ENSP00000343408.4:p.Ter303GlnextTer2
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: stop_lost
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.970T>C
  hgvsp: ENSP00000417914.1:p.Ter324GlnextTer2
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: stop lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4793
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5356
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17417
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2293
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3569
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2726
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genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2826
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14415
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ter324GlnextTer2
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

X-15301630-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301630
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301630
    reference: chr 0
allele count: 2
allele frequency: 2.279098388677439e-5
allele num: 87754
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.969A>G
  hgvsp: ENST00000480796.1:c.969A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.906A>G
  hgvsp: ENST00000537676.1:c.906A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.918A>G
  hgvsp: ENST00000380470.3:c.918A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.906A>G
  hgvsp: ENST00000344384.4:c.906A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*412A>G
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13017
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 463
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5355
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genotype quality: GenotypeQuality
  all individuals: 4
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genotype quality: GenotypeQuality
  all individuals: 12
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3570
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2726
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genotype quality: GenotypeQuality
  all individuals: 25279
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 14413
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genotype quality: GenotypeQuality
  all individuals: 2
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genotype quality: GenotypeQuality
  all individuals: 0
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Gln323Gln
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

X-15301631-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301631
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301631
    reference: chr 0
allele count: 1
allele frequency: 1.13954919433872e-5
allele num: 87754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.905A>G
  hgvsp: ENSP00000343408.4:p.Gln302Arg
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.905A>G
  hgvsp: ENSP00000445465.1:p.Gln302Arg
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.968A>G
  hgvsp: ENSP00000417914.1:p.Gln323Arg
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*411A>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.917A>G
  hgvsp: ENSP00000369837.3:p.Gln306Arg
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17422
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6631
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4795
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 636
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8078
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2726
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2294
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1485
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3571
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
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genotype quality: GenotypeQuality
  all individuals: 0
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gln323Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

X-15301634-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301634
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301634
    reference: chr 0
allele count: 3
allele frequency: 3.4186086262891e-5
allele num: 87755
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*408A>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.902A>G
  hgvsp: ENSP00000445465.1:p.Tyr301Cys
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.965A>G
  hgvsp: ENSP00000417914.1:p.Tyr322Cys
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.914A>G
  hgvsp: ENSP00000369837.3:p.Tyr305Cys
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.902A>G
  hgvsp: ENSP00000343408.4:p.Tyr301Cys
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 445
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13019
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8079
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2828
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1485
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25285
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Tyr322Cys
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

X-15301635-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301635
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301635
    reference: chr 0
allele count: 2
allele frequency: 2.278994507623237e-5
allele num: 87758
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.901T>C
  hgvsp: ENSP00000445465.1:p.Tyr301His
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.901T>C
  hgvsp: ENSP00000343408.4:p.Tyr301His
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*407T>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.913T>C
  hgvsp: ENSP00000369837.3:p.Tyr305His
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.964T>C
  hgvsp: ENSP00000417914.1:p.Tyr322His
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13023
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17428
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1485
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2726
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2829
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25287
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3571
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Tyr322His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

X-15301636-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301636
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301636
    reference: chr 0
allele count: 2
allele frequency: 2.278994507623237e-5
allele num: 87758
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.912A>G
  hgvsp: ENST00000380470.3:c.912A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.900A>G
  hgvsp: ENST00000537676.1:c.900A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*406A>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.900A>G
  hgvsp: ENST00000344384.4:c.900A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.963A>G
  hgvsp: ENST00000480796.1:c.963A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4795
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17430
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3571
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2726
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8080
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14408
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2294
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu321Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

X-15301641-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301641
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301641
    reference: chr 0
allele count: 2
allele frequency: 2.278916603046912e-5
allele num: 87761
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.895C>T
  hgvsp: ENSP00000343408.4:p.Leu299Phe
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.958C>T
  hgvsp: ENSP00000417914.1:p.Leu320Phe
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.895C>T
  hgvsp: ENSP00000445465.1:p.Leu299Phe
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.907C>T
  hgvsp: ENSP00000369837.3:p.Leu303Phe
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*401C>T
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2020
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13022
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4794
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5350
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6630
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25293
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8084
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3571
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2294
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2727
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Leu320Phe
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

X-15301646-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301646
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301646
    reference: chr 0
allele count: 1
allele frequency: 1.139458301523456e-5
allele num: 87761
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*396G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.953G>A
  hgvsp: ENSP00000417914.1:p.Arg318Gln
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.902G>A
  hgvsp: ENSP00000369837.3:p.Arg301Gln
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.890G>A
  hgvsp: ENSP00000445465.1:p.Arg297Gln
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.890G>A
  hgvsp: ENSP00000343408.4:p.Arg297Gln
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
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genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 2.25e1
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genotype depth: GenotypeDepth
  all individuals: 2020
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genotype depth: GenotypeDepth
  all individuals: 2849
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1
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genotype depth: GenotypeDepth
  all individuals: 635
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genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
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genotype depth: GenotypeDepth
  all individuals: 17439
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 440
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genotype depth: GenotypeDepth
  all individuals: 163
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genotype depth: GenotypeDepth
  all individuals: 463
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2829
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg318Gln
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP

X-15301650-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301650
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301650
    reference: chr 0
allele count: 5
allele frequency: 5.697226590095942e-5
allele num: 87762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.886G>A
  hgvsp: ENSP00000445465.1:p.Glu296Lys
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.949G>A
  hgvsp: ENSP00000417914.1:p.Glu317Lys
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.886G>A
  hgvsp: ENSP00000343408.4:p.Glu296Lys
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.898G>A
  hgvsp: ENSP00000369837.3:p.Glu300Lys
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*392G>A
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17444
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
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genotype depth: GenotypeDepth
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  bin: 5.25e1
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genotype depth: GenotypeDepth
  all individuals: 6631
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 9.75e1
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genotype depth: GenotypeDepth
  all individuals: 214
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2728
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genotype quality: GenotypeQuality
  all individuals: 3571
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 14405
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu317Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: C
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

X-15301659-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301659
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301659
    reference: chr 0
allele count: 1
allele frequency: 1.139432334810797e-5
allele num: 87763
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.877G>C
  hgvsp: ENSP00000445465.1:p.Glu293Gln
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.940G>C
  hgvsp: ENSP00000417914.1:p.Glu314Gln
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.889G>C
  hgvsp: ENSP00000369837.3:p.Glu297Gln
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.877G>C
  hgvsp: ENSP00000343408.4:p.Glu293Gln
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*383G>C
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 334
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
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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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1486
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  variant carriers: 0
hgvs: p.Glu314Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: QD

X-15301661-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301661
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301661
    reference: chr 0
allele count: 1
allele frequency: 1.139432334810797e-5
allele num: 87763
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.875C>T
  hgvsp: ENSP00000445465.1:p.Pro292Leu
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*381C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.938C>T
  hgvsp: ENSP00000417914.1:p.Pro313Leu
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.887C>T
  hgvsp: ENSP00000369837.3:p.Pro296Leu
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.875C>T
  hgvsp: ENSP00000343408.4:p.Pro292Leu
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
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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
  all individuals: 1479
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 4.75e1
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genotype quality: GenotypeQuality
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  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2729
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3571
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2293
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro313Leu
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

X-15301672-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301672
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301672
    reference: chr 0
allele count: 3
allele frequency: 3.418258055694818e-5
allele num: 87764
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*370G>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.864G>C
  hgvsp: ENSP00000445465.1:p.Lys288Asn
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.927G>C
  hgvsp: ENSP00000417914.1:p.Lys309Asn
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.864G>C
  hgvsp: ENSP00000343408.4:p.Lys288Asn
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.876G>C
  hgvsp: ENSP00000369837.3:p.Lys292Asn
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 435
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  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 463
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genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.25e1
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genotype depth: GenotypeDepth
  all individuals: 0
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
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genotype depth: GenotypeDepth
  all individuals: 13028
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 2849
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2829
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genotype quality: GenotypeQuality
  all individuals: 8084
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys309Asn
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

X-15301686-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301686
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301686
    reference: chr 0
allele count: 1
allele frequency: 1.139419351898273e-5
allele num: 87764
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.862C>G
  hgvsp: ENSP00000369837.3:p.Gln288Glu
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.913C>G
  hgvsp: ENSP00000417914.1:p.Gln305Glu
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.850C>G
  hgvsp: ENSP00000445465.1:p.Gln284Glu
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*356C>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.850C>G
  hgvsp: ENSP00000343408.4:p.Gln284Glu
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13028
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
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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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  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 0
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genotype quality: GenotypeQuality
  all individuals: 2293
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln305Glu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

X-15301692-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301692
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301692
    reference: chr 0
allele count: 1
allele frequency: 1.139432334810797e-5
allele num: 87763
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*350T>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.844T>C
  hgvsp: ENSP00000445465.1:p.Cys282Arg
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.856T>C
  hgvsp: ENSP00000369837.3:p.Cys286Arg
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.844T>C
  hgvsp: ENSP00000343408.4:p.Cys282Arg
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.907T>C
  hgvsp: ENSP00000417914.1:p.Cys303Arg
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
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genotype depth: GenotypeDepth
  all individuals: 162
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
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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
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2829
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genotype quality: GenotypeQuality
  all individuals: 2728
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Cys303Arg
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP

X-15301697-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301697
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301697
    reference: chr 0
allele count: 1
allele frequency: 1.139458301523456e-5
allele num: 87761
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.839G>A
  hgvsp: ENSP00000343408.4:p.Arg280Gln
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.839G>A
  hgvsp: ENSP00000445465.1:p.Arg280Gln
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.851G>A
  hgvsp: ENSP00000369837.3:p.Arg284Gln
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.902G>A
  hgvsp: ENSP00000417914.1:p.Arg301Gln
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*345G>A
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
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genotype depth: GenotypeDepth
  all individuals: 13024
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 6629
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 987
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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
  all individuals: 4
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genotype depth: GenotypeDepth
  all individuals: 334
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
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genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8087
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25298
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1486
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2293
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg301Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum

X-15301698-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301698
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301698
    reference: chr 0
allele count: 3
allele frequency: 3.418374904570367e-5
allele num: 87761
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.838C>G
  hgvsp: ENSP00000445465.1:p.Arg280Gly
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.838C>G
  hgvsp: ENSP00000343408.4:p.Arg280Gly
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.850C>G
  hgvsp: ENSP00000369837.3:p.Arg284Gly
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*344C>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.901C>G
  hgvsp: ENSP00000417914.1:p.Arg301Gly
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3571
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8085
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2292
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2829
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg301Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

X-15301698-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301698
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301698
    reference: chr 0
allele count: 24
allele frequency: 2.734699923656294e-4
allele num: 87761
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*344C>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.901C>A
  hgvsp: ENST00000480796.1:c.901C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.850C>A
  hgvsp: ENST00000380470.3:c.850C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.838C>A
  hgvsp: ENST00000344384.4:c.838C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.838C>A
  hgvsp: ENST00000537676.1:c.838C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13026
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2292
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2829
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
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genotype quality: GenotypeQuality
  all individuals: 8
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3571
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2728
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg301Arg
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

X-15301700-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301700
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301700
    reference: chr 0
allele count: 1
allele frequency: 1.139458301523456e-5
allele num: 87761
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.848G>T
  hgvsp: ENSP00000369837.3:p.Gly283Val
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.836G>T
  hgvsp: ENSP00000445465.1:p.Gly279Val
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*342G>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.899G>T
  hgvsp: ENSP00000417914.1:p.Gly300Val
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.836G>T
  hgvsp: ENSP00000343408.4:p.Gly279Val
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13030
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2729
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  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: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3573
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2831
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly300Val
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

X-15301701-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301701
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301701
    reference: chr 0
allele count: 1
allele frequency: 1.139458301523456e-5
allele num: 87761
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.835G>C
  hgvsp: ENSP00000343408.4:p.Gly279Arg
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*341G>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.898G>C
  hgvsp: ENSP00000417914.1:p.Gly300Arg
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.847G>C
  hgvsp: ENSP00000369837.3:p.Gly283Arg
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.835G>C
  hgvsp: ENSP00000445465.1:p.Gly279Arg
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3570
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14391
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8086
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2830
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2292
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly300Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

X-15301701-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301701
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301701
    reference: chr 0
allele count: 72
allele frequency: 8.204099770968881e-4
allele num: 87761
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.847G>A
  hgvsp: ENSP00000369837.3:p.Gly283Ser
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.898G>A
  hgvsp: ENSP00000417914.1:p.Gly300Ser
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.835G>A
  hgvsp: ENSP00000445465.1:p.Gly279Ser
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.835G>A
  hgvsp: ENSP00000343408.4:p.Gly279Ser
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*341G>A
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 17447
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4797
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13028
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 425
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  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 0
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2849
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
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  variant carriers: 1
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2292
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2830
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8086
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly300Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

X-15301702-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301702
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301702
    reference: chr 0
allele count: 2
allele frequency: 2.278916603046912e-5
allele num: 87761
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.897C>T
  hgvsp: ENST00000480796.1:c.897C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*340C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.834C>T
  hgvsp: ENST00000344384.4:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.846C>T
  hgvsp: ENST00000380470.3:c.846C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.834C>T
  hgvsp: ENST00000537676.1:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3872
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
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genotype depth: GenotypeDepth
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  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6644
  bin: 3.75e1
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genotype depth: GenotypeDepth
  all individuals: 382
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  variant carriers: 2
genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
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genotype quality: GenotypeQuality
  all individuals: 2727
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3576
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8097
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu299Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

X-15301708-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301708
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301708
    reference: chr 0
allele count: 1
allele frequency: 1.139458301523456e-5
allele num: 87761
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.828G>A
  hgvsp: ENST00000344384.4:c.828G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*334G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.891G>A
  hgvsp: ENST00000480796.1:c.891G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.840G>A
  hgvsp: ENST00000380470.3:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.828G>A
  hgvsp: ENST00000537676.1:c.828G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
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genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3577
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys297Lys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

X-15301708-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301708
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301708
    reference: chr 0
allele count: 1
allele frequency: 1.139458301523456e-5
allele num: 87761
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.891G>C
  hgvsp: ENSP00000417914.1:p.Lys297Asn
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.840G>C
  hgvsp: ENSP00000369837.3:p.Lys280Asn
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*334G>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.828G>C
  hgvsp: ENSP00000445465.1:p.Lys276Asn
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.828G>C
  hgvsp: ENSP00000343408.4:p.Lys276Asn
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3873
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5347
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25334
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2833
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3577
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14333
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1488
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys297Asn
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

X-15301712-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301712
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301712
    reference: chr 0
allele count: 1
allele frequency: 1.13947128532361e-5
allele num: 87760
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.887G>A
  hgvsp: ENSP00000417914.1:p.Arg296Gln
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.824G>A
  hgvsp: ENSP00000445465.1:p.Arg275Gln
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*330G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.824G>A
  hgvsp: ENSP00000343408.4:p.Arg275Gln
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.836G>A
  hgvsp: ENSP00000369837.3:p.Arg279Gln
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3875
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
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genotype depth: GenotypeDepth
  all individuals: 986
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genotype depth: GenotypeDepth
  all individuals: 17465
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genotype depth: GenotypeDepth
  all individuals: 6645
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genotype quality: GenotypeQuality
  all individuals: 3
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genotype quality: GenotypeQuality
  all individuals: 0
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genotype quality: GenotypeQuality
  all individuals: 3575
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genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 14333
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 1
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genotype quality: GenotypeQuality
  all individuals: 2
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genotype quality: GenotypeQuality
  all individuals: 25335
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1488
  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg296Gln
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

X-15301713-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301713
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301713
    reference: chr 0
allele count: 23
allele frequency: 2.620813819665219e-4
allele num: 87759
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.823C>T
  hgvsp: ENSP00000445465.1:p.Arg275Trp
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*329C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.886C>T
  hgvsp: ENSP00000417914.1:p.Arg296Trp
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.835C>T
  hgvsp: ENSP00000369837.3:p.Arg279Trp
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.823C>T
  hgvsp: ENSP00000343408.4:p.Arg275Trp
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 379
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 3874
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2850
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25334
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2290
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2831
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
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genotype quality: GenotypeQuality
  all individuals: 8096
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1488
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 5
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg296Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

X-15301715-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301715
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301715
    reference: chr 0
allele count: 2
allele frequency: 2.278968538839321e-5
allele num: 87759
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.884T>C
  hgvsp: ENSP00000417914.1:p.Val295Ala
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.833T>C
  hgvsp: ENSP00000369837.3:p.Val278Ala
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.821T>C
  hgvsp: ENSP00000445465.1:p.Val274Ala
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*327T>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.821T>C
  hgvsp: ENSP00000343408.4:p.Val274Ala
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17475
  bin: 2.75e1
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genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13046
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
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genotype depth: GenotypeDepth
  all individuals: 159
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genotype depth: GenotypeDepth
  all individuals: 360
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2833
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3577
  bin: 7.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1
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genotype quality: GenotypeQuality
  all individuals: 25346
  bin: 6.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14315
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genotype quality: GenotypeQuality
  all individuals: 16
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 0
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2292
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Val295Ala
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD

X-15301718-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301718
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301718
    reference: chr 0
allele count: 5
allele frequency: 5.697616117416473e-5
allele num: 87756
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.818G>A
  hgvsp: ENSP00000445465.1:p.Cys273Tyr
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*324G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.881G>A
  hgvsp: ENSP00000417914.1:p.Cys294Tyr
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.818G>A
  hgvsp: ENSP00000343408.4:p.Cys273Tyr
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.830G>A
  hgvsp: ENSP00000369837.3:p.Cys277Tyr
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13045
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25334
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14313
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2292
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2727
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Cys294Tyr
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff

X-15301724-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301724
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301724
    reference: chr 0
allele count: 1
allele frequency: 1.139614126656714e-5
allele num: 87749
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*318G>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.824G>T
  hgvsp: ENSP00000369837.3:p.Arg275Leu
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.812G>T
  hgvsp: ENSP00000343408.4:p.Arg271Leu
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.812G>T
  hgvsp: ENSP00000445465.1:p.Arg271Leu
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.875G>T
  hgvsp: ENSP00000417914.1:p.Arg292Leu
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 2831
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2293
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8092
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14308
  bin: 9.75e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg292Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

X-15301724-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301724
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301724
    reference: chr 0
allele count: 6
allele frequency: 6.837684759940284e-5
allele num: 87749
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.824G>C
  hgvsp: ENSP00000369837.3:p.Arg275Pro
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.812G>C
  hgvsp: ENSP00000343408.4:p.Arg271Pro
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.812G>C
  hgvsp: ENSP00000445465.1:p.Arg271Pro
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.875G>C
  hgvsp: ENSP00000417914.1:p.Arg292Pro
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*318G>C
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14308
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8092
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3576
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2728
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg292Pro
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

X-15301724-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301724
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301724
    reference: chr 0
allele count: 1
allele frequency: 1.139614126656714e-5
allele num: 87749
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.875G>A
  hgvsp: ENSP00000417914.1:p.Arg292His
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.812G>A
  hgvsp: ENSP00000343408.4:p.Arg271His
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.812G>A
  hgvsp: ENSP00000445465.1:p.Arg271His
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*318G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.824G>A
  hgvsp: ENSP00000369837.3:p.Arg275His
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14308
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2831
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25332
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2728
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg292His
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

X-15301725-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301725
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301725
    reference: chr 0
allele count: 6
allele frequency: 6.837918537597155e-5
allele num: 87746
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.811C>T
  hgvsp: ENSP00000445465.1:p.Arg271Cys
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.823C>T
  hgvsp: ENSP00000369837.3:p.Arg275Cys
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.811C>T
  hgvsp: ENSP00000343408.4:p.Arg271Cys
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*317C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.874C>T
  hgvsp: ENSP00000417914.1:p.Arg292Cys
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6647
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2293
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25327
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3575
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8090
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg292Cys
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

X-15301725-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301725
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301725
    reference: chr 0
allele count: 2
allele frequency: 2.279306179199052e-5
allele num: 87746
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*317C>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.874C>G
  hgvsp: ENSP00000417914.1:p.Arg292Gly
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.823C>G
  hgvsp: ENSP00000369837.3:p.Arg275Gly
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.811C>G
  hgvsp: ENSP00000445465.1:p.Arg271Gly
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.811C>G
  hgvsp: ENSP00000343408.4:p.Arg271Gly
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6647
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8090
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
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genotype quality: GenotypeQuality
  all individuals: 5
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2726
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genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
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genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25327
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg292Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ

X-15301725-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301725
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301725
    reference: chr 0
allele count: 1
allele frequency: 1.139653089599526e-5
allele num: 87746
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.811C>A
  hgvsp: ENSP00000445465.1:p.Arg271Ser
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.874C>A
  hgvsp: ENSP00000417914.1:p.Arg292Ser
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*317C>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.823C>A
  hgvsp: ENSP00000369837.3:p.Arg275Ser
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.811C>A
  hgvsp: ENSP00000343408.4:p.Arg271Ser
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6647
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2853
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13036
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8090
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genotype quality: GenotypeQuality
  all individuals: 6
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14297
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2726
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
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genotype quality: GenotypeQuality
  all individuals: 0
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genotype quality: GenotypeQuality
  all individuals: 5
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genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg292Ser
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

X-15301727-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301727
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301727
    reference: chr 0
allele count: 1
allele frequency: 1.139666077839193e-5
allele num: 87745
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.809G>C
  hgvsp: ENSP00000343408.4:p.Cys270Ser
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.821G>C
  hgvsp: ENSP00000369837.3:p.Cys274Ser
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.872G>C
  hgvsp: ENSP00000417914.1:p.Cys291Ser
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.809G>C
  hgvsp: ENSP00000445465.1:p.Cys270Ser
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*315G>C
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5351
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3575
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 2293
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genotype quality: GenotypeQuality
  all individuals: 0
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2725
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 2831
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Cys291Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

X-15301728-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301728
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301728
    reference: chr 0
allele count: 2
allele frequency: 2.279384110413366e-5
allele num: 87743
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.808T>C
  hgvsp: ENSP00000343408.4:p.Cys270Arg
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.820T>C
  hgvsp: ENSP00000369837.3:p.Cys274Arg
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*314T>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.871T>C
  hgvsp: ENSP00000417914.1:p.Cys291Arg
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.808T>C
  hgvsp: ENSP00000445465.1:p.Cys270Arg
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
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genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2017
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 2
genotype quality: GenotypeQuality
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  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 7.75e1
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genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25347
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Cys291Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

X-15301740-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301740
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301740
    reference: chr 0
allele count: 2
allele frequency: 2.280397701359117e-5
allele num: 87704
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.796C>G
  hgvsp: ENSP00000343408.4:p.Leu266Val
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*302C>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.808C>G
  hgvsp: ENSP00000369837.3:p.Leu270Val
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.859C>G
  hgvsp: ENSP00000417914.1:p.Leu287Val
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.796C>G
  hgvsp: ENSP00000445465.1:p.Leu266Val
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13018
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6643
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2851
  bin: 5.25e1
  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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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
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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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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu287Val
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

X-15301751-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301751
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301751
    reference: chr 0
allele count: 1
allele frequency: 1.141695875052804e-5
allele num: 87589
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*291G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.797G>A
  hgvsp: ENSP00000369837.3:p.Gly266Asp
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.785G>A
  hgvsp: ENSP00000445465.1:p.Gly262Asp
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.848G>A
  hgvsp: ENSP00000417914.1:p.Gly283Asp
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.785G>A
  hgvsp: ENSP00000343408.4:p.Gly262Asp
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 6.25e1
  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gly283Asp
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: C
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum

X-15301761-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301761
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301761
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 87444
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*291-10T>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.785-10T>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.848-10T>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.785-10T>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.797-10T>G
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 156
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: A
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

X-15301772-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301772
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301772
    reference: chr 0
allele count: 11
allele frequency: 1.261815178489492e-4
allele num: 87176
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.785-21C>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.797-21C>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.848-21C>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.785-21C>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*291-21C>A
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16057
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1995
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  bin: 5.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 4667
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 980
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genotype depth: GenotypeDepth
  all individuals: 625
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genotype depth: GenotypeDepth
  all individuals: 214
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 337
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 7296
  bin: 6.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 1.25e1
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genotype quality: GenotypeQuality
  all individuals: 2740
  bin: 8.25e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1832
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1434
  bin: 8.75e1
  variant carriers: 1
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

X-15301774-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301774
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301774
    reference: chr 0
allele count: 1
allele frequency: 1.148184719957747e-5
allele num: 87094
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.785-23C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.848-23C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.797-23C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*291-23C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.785-23C>T
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
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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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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 214
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1432
  bin: 8.75e1
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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
  all individuals: 141
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genotype quality: GenotypeQuality
  all individuals: 21981
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

X-15301779-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301779
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301779
    reference: chr 0
allele count: 1
allele frequency: 1.15065529819232e-5
allele num: 86907
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*291-28G>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.848-28G>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.785-28G>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.785-28G>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.797-28G>C
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10630
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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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  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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  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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 294
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: QD

X-15301782-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301782
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301782
    reference: chr 0
allele count: 3
allele frequency: 3.457336467985064e-5
allele num: 86772
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.785-31G>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.848-31G>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*291-31G>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.797-31G>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.785-31G>T
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4216
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 1
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
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2236
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff

X-15301786-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301786
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301786
    reference: chr 0
allele count: 1
allele frequency: 1.156483826573685e-5
allele num: 86469
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*291-35C>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.785-35C>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.848-35C>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
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  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.785-35C>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.797-35C>G
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 6.25e1
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num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

X-15301791-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301791
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301791
    reference: chr 0
allele count: 1
allele frequency: 1.159796803600009e-5
allele num: 86222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.785-40C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.785-40C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
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  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*291-40C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
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  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.797-40C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.848-40C>T
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: intron
filter: PASS
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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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

X-15301798-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301798
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301798
    reference: chr 0
allele count: 1
allele frequency: 1.174798228404272e-5
allele num: 85121
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*291-47C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.797-47C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.848-47C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.785-47C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
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  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.785-47C>T
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum

X-15301801-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015301801
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015301801
    reference: chr 0
allele count: 1
allele frequency: 1.17638754911418e-5
allele num: 85006
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.848-50C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.785-50C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.785-50C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.797-50C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
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  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*291-50C>T
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: intron
filter: PASS
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 quality: GenotypeQuality
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num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

X-15305962-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015305962
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015305962
    reference: chr 0
allele count: 3
allele frequency: 3.739669163934631e-5
allele num: 80221
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.847+41A>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.796+41A>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*290+41A>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.784+41A>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.784+41A>G
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
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  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

X-15305965-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015305965
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015305965
    reference: chr 0
allele count: 1
allele frequency: 1.245748881940378e-5
allele num: 80273
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.784+38C>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.847+38C>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.784+38C>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*290+38C>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.796+38C>A
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

X-15305966-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015305966
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015305966
    reference: chr 0
allele count: 1
allele frequency: 1.247084938955192e-5
allele num: 80187
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.784+37G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*290+37G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.784+37G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.847+37G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.796+37G>A
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

X-15305983-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015305983
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015305983
    reference: chr 0
allele count: 7
allele frequency: 8.647313156269301e-5
allele num: 80950
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.784+20C>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.784+20C>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.796+20C>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.847+20C>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*290+20C>G
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: intron
filter: PASS
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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

X-15305987-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015305987
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015305987
    reference: chr 0
allele count: 7
allele frequency: 8.648274669203493e-5
allele num: 80941
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*290+16G>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.847+16G>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.796+16G>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.784+16G>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.784+16G>T
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 2449
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10876
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7384
  bin: 3.25e1
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genotype depth: GenotypeDepth
  all individuals: 4455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1506
  bin: 3.25e1
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genotype quality: GenotypeQuality
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  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 1637
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1183
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25858
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 2207
  bin: 7.25e1
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genotype quality: GenotypeQuality
  all individuals: 1182
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1163
  bin: 8.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

X-15305989-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015305989
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015305989
    reference: chr 0
allele count: 0
allele frequency: 0.0e0
allele num: 81369
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*290+14G>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.796+14G>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.847+14G>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.784+14G>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.784+14G>T
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
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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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  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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  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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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 7.25e1
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4297
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 6.25e1
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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: 417
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1083
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

X-15305994-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015305994
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015305994
    reference: chr 0
allele count: 1
allele frequency: 1.22276295517351e-5
allele num: 81782
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.796+9G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.784+9G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*290+9G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.784+9G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.847+9G>A
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11597
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
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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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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
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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
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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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1656
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum

X-15305997-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015305997
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015305997
    reference: chr 0
allele count: 50
allele frequency: 6.098602200375674e-4
allele num: 81986
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*290+6C>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.784+6C>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.796+6C>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.847+6C>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.784+6C>A
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 248
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  variant carriers: 5
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: 6
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 342
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  variant carriers: 2
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 3
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 quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 737
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1182
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 1067
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
hgvs: c.847+6C>A
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

X-15306007-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015306007
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015306006
    reference: chr 0
allele count: 1
allele frequency: 1.208926714862545e-5
allele num: 82718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.779delG
  hgvsp: ENSP00000445465.1:p.Arg260LeufsTer68
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.779delG
  hgvsp: ENSP00000343408.4:p.Arg260LeufsTer68
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.791delG
  hgvsp: ENSP00000369837.3:p.Arg264LeufsTer68
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*285delG
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.842delG
  hgvsp: ENSP00000417914.1:p.Arg281LeufsTer68
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7574
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3972
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28524
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 881
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2432
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2303
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1654
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3091
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg281LeufsTer68
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: AC
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

X-15306009-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015306009
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015306009
    reference: chr 0
allele count: 3
allele frequency: 3.617595986880185e-5
allele num: 82928
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.778C>T
  hgvsp: ENSP00000343408.4:p.Arg260Cys
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.778C>T
  hgvsp: ENSP00000445465.1:p.Arg260Cys
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.790C>T
  hgvsp: ENSP00000369837.3:p.Arg264Cys
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.841C>T
  hgvsp: ENSP00000417914.1:p.Arg281Cys
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*284C>T
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 872
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22027
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 951
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7655
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 803
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1188
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 2435
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1656
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg281Cys
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

X-15306010-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015306010
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015306010
    reference: chr 0
allele count: 1
allele frequency: 1.20410841792195e-5
allele num: 83049
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.840C>T
  hgvsp: ENST00000480796.1:c.840C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.777C>T
  hgvsp: ENST00000344384.4:c.777C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.777C>T
  hgvsp: ENST00000537676.1:c.777C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*283C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.789C>T
  hgvsp: ENST00000380470.3:c.789C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22111
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12689
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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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  bin: 6.25e1
  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: 340
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 780
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6616
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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: 116
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu280Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

X-15306012-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015306012
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015306012
    reference: chr 0
allele count: 1
allele frequency: 1.202110906752257e-5
allele num: 83187
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.775C>T
  hgvsp: ENSP00000445465.1:p.Leu259Phe
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.787C>T
  hgvsp: ENSP00000369837.3:p.Leu263Phe
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*281C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.838C>T
  hgvsp: ENSP00000417914.1:p.Leu280Phe
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.775C>T
  hgvsp: ENSP00000343408.4:p.Leu259Phe
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2431
  bin: 4.25e1
  variant carriers: 0
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
  all individuals: 1812
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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: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 391
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29577
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1654
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3843
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6097
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2435
  bin: 8.25e1
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genotype quality: GenotypeQuality
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  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu280Phe
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD

X-15306028-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015306028
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015306028
    reference: chr 0
allele count: 4
allele frequency: 4.738831167292587e-5
allele num: 84409
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.759G>A
  hgvsp: ENST00000344384.4:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.759G>A
  hgvsp: ENST00000537676.1:c.759G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*265G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.771G>A
  hgvsp: ENST00000380470.3:c.771G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.822G>A
  hgvsp: ENST00000480796.1:c.822G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 4.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 192
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genotype quality: GenotypeQuality
  all individuals: 3111
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val274Val
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ

X-15306030-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015306030
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015306030
    reference: chr 0
allele count: 3
allele frequency: 3.545386860796294e-5
allele num: 84617
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.757G>A
  hgvsp: ENSP00000445465.1:p.Val253Met
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.757G>A
  hgvsp: ENSP00000343408.4:p.Val253Met
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*263G>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.769G>A
  hgvsp: ENSP00000369837.3:p.Val257Met
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.820G>A
  hgvsp: ENSP00000417914.1:p.Val274Met
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Val274Met
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ReadPosRankSum

X-15306031-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015306031
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015306031
    reference: chr 0
allele count: 2
allele frequency: 2.359213909925213e-5
allele num: 84774
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.756C>T
  hgvsp: ENST00000344384.4:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.768C>T
  hgvsp: ENST00000380470.3:c.768C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.819C>T
  hgvsp: ENST00000480796.1:c.819C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*262C>T
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.756C>T
  hgvsp: ENST00000537676.1:c.756C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
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  bin: 2.25e1
  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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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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hgvs: p.Ser273Ser
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

X-15306058-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015306058
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015306058
    reference: chr 0
allele count: 4
allele frequency: 4.600768328310828e-5
allele num: 86942
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.741G>A
  hgvsp: ENST00000380470.3:c.741G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.792G>A
  hgvsp: ENST00000480796.1:c.792G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.729G>A
  hgvsp: ENST00000537676.1:c.729G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.729G>A
  hgvsp: ENST00000344384.4:c.729G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*235G>A
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
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  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
  all individuals: 6500
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1195
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala264Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP

X-15306059-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015306059
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015306059
    reference: chr 0
allele count: 1
allele frequency: 1.148989463766617e-5
allele num: 87033
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.728C>A
  hgvsp: ENSP00000445465.1:p.Ala243Glu
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.728C>A
  hgvsp: ENSP00000343408.4:p.Ala243Glu
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*234C>A
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.740C>A
  hgvsp: ENSP00000369837.3:p.Ala247Glu
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.791C>A
  hgvsp: ENSP00000417914.1:p.Ala264Glu
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25185
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15235
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7970
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3156
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2386
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1664
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 752
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6512
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35316
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala264Glu
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: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD

X-15306061-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015306061
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015306061
    reference: chr 0
allele count: 2
allele frequency: 2.295288919492741e-5
allele num: 87135
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.726T>C
  hgvsp: ENST00000537676.1:c.726T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*232T>C
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.789T>C
  hgvsp: ENST00000480796.1:c.789T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.738T>C
  hgvsp: ENST00000380470.3:c.738T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.726T>C
  hgvsp: ENST00000344384.4:c.726T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4293
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 870
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2393
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1196
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35550
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6622
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Ser263Ser
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

X-15306063-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 24015306063
    reference: chr 0
  end: Position
    type: ExactPosition
    position: 24015306063
    reference: chr 0
allele count: 1481
allele frequency: 1.698277641446689e-2
allele num: 87206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000369837
  ensembl transcript: ENST00000380470
  gene symbol: ASB11
  hgvsc: ENST00000380470.3:c.736A>G
  hgvsp: ENSP00000369837.3:p.Ser246Gly
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000445465
  ensembl transcript: ENST00000537676
  gene symbol: ASB11
  hgvsc: ENST00000537676.1:c.724A>G
  hgvsp: ENSP00000445465.1:p.Ser242Gly
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000417914
  ensembl transcript: ENST00000480796
  gene symbol: ASB11
  hgvsc: ENST00000480796.1:c.787A>G
  hgvsp: ENSP00000417914.1:p.Ser263Gly
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000419385
  ensembl transcript: ENST00000485437
  gene symbol: ASB11
  hgvsc: ENST00000485437.2:c.*230A>G
  variant of: http://identifiers.org/hgnc/17186
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000165192
  ensembl protein: ENSP00000343408
  ensembl transcript: ENST00000344384
  gene symbol: ASB11
  hgvsc: ENST00000344384.4:c.724A>G
  hgvsp: ENSP00000343408.4:p.Ser242Gly
  variant of: http://identifiers.org/hgnc/17186
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 9.75e1
  variant carriers: 497
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 936
  bin: 5.25e1
  variant carriers: 94
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 24914
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 8.75e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 15083
  bin: 2.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 7751
  bin: 3.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 4.25e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 6.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 6.75e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 7.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 5.75e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 4.75e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.25e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 8.25e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 4210
  bin: 3.75e1
  variant carriers: 55
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 3.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1606
  bin: 9.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 2381
  bin: 8.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 2.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 2307
  bin: 7.25e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 7504
  bin: 9.75e1
  variant carriers: 1363
hgvs: p.Ser263Gly
num of homozygotes: 21
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
reference allele: T

GenotypeQuality
all individuals: 1796
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6403
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2422
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1790
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4003
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6831
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.186174631629575e-5
allele num: 45742
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 553
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9102
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4351
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.843e0

VQSLOD
type: SiteQuality
SIO_000300: -2.073e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 1.458555e6

MQ
type: SiteQuality
SIO_000300: 5.038e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.383e1

MQRankSum
type: SiteQuality
SIO_000300: 2.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.7e-1

GenotypeQuality
all individuals: 295
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47966
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10072
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.34796900680911e-4
allele num: 8518
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.126e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.522e0

DP
type: SiteQuality
SIO_000300: 2.65929e6

MQRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.878e1

FS
type: SiteQuality
SIO_000300: 8.86e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

GenotypeQuality
all individuals: 156
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7458
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47969
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.929500546122529e-5
allele num: 10071
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 3.323e1

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

DP
type: SiteQuality
SIO_000300: 2.662224e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.13e-2

GenotypeQuality
all individuals: 7477
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2543
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10073
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8517
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 631
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.084723148765844e-5
allele num: 47968
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.665865e6

MQ
type: SiteQuality
SIO_000300: 5.972e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.13e-1

FS
type: SiteQuality
SIO_000300: 1.368e0

MQRankSum
type: SiteQuality
SIO_000300: -4.54e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.332e0

QD
type: SiteQuality
SIO_000300: 2.78e1

GenotypeQuality
all individuals: 87
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1378
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2632
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10090
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.084505867884018e-5
allele num: 47973
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

DP
type: SiteQuality
SIO_000300: 2.668818e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.183e0

QD
type: SiteQuality
SIO_000300: 1.107e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 7.4e-2

MQ
type: SiteQuality
SIO_000300: 5.987e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.639e0

GenotypeQuality
all individuals: 2631
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47975
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.506931886678722e-4
allele num: 6636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10093
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 9.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.911e0

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

QD
type: SiteQuality
SIO_000300: 1.346e1

FS
type: SiteQuality
SIO_000300: 9.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e-1

DP
type: SiteQuality
SIO_000300: 2.669684e6

MQ
type: SiteQuality
SIO_000300: 5.904e1

VQSLOD
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 2634
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10118
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.521953510213665e-4
allele num: 8518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47987
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.745e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.749999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.45e-1

FS
type: SiteQuality
SIO_000300: 3.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.4e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

DP
type: SiteQuality
SIO_000300: 2.673647e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.788e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.96e-1

GenotypeQuality
all individuals: 17594
bin: 9.75e1
variant carriers: 4430

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 3

GenotypeQuality
all individuals: 7517
bin: 6.75e1
variant carriers: 2

Other
type: Population
allele count: 39
allele frequency: 6.161137440758294e-2
allele num: 633
num of homozygotes: 1

Latino
type: Population
allele count: 252
allele frequency: 2.702702702702703e-2
allele num: 9324
num of homozygotes: 5

South Asian
type: Population
allele count: 393
allele frequency: 3.883782982508153e-2
allele num: 10119
num of homozygotes: 7

African
type: Population
allele count: 515
allele frequency: 6.046730069273219e-2
allele num: 8517
num of homozygotes: 13

European (Finnish)
type: Population
allele count: 167
allele frequency: 3.686534216335541e-2
allele num: 4530
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3216
allele frequency: 6.701675418854713e-2
allele num: 47988
num of homozygotes: 79

QD
type: SiteQuality
SIO_000300: 1.827e1

MQ
type: SiteQuality
SIO_000300: 5.962e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.613e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.011e1

MQRankSum
type: SiteQuality
SIO_000300: 1.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.725e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.951247e6

GenotypeQuality
all individuals: 25271
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2294
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3570
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2727
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14418
bin: 9.75e1
variant carriers: 3

South Asian
type: Population
allele count: 2
allele frequency: 1.975698903487109e-4
allele num: 10123
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.072501072501073e-4
allele num: 9324
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47990
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.26e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.453e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.87e0

DP
type: SiteQuality
SIO_000300: 2.254049e6

MQRankSum
type: SiteQuality
SIO_000300: 1.7e0

QD
type: SiteQuality
SIO_000300: 3.32e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.08e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8077
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 25281
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.251302354657221e-5
allele num: 47990
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10123
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.736e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.92e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.87e0

MQRankSum
type: SiteQuality
SIO_000300: -4.86e-1

MQ
type: SiteQuality
SIO_000300: 5.945e1

DP
type: SiteQuality
SIO_000300: 2.253971e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.4e-1

QD
type: SiteQuality
SIO_000300: 2.463e1

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1485
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2827
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2294
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47990
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.207505518763797e-4
allele num: 4530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.878494517435543e-5
allele num: 10123
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.253537e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

FS
type: SiteQuality
SIO_000300: 7.058e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.9e0

MQ
type: SiteQuality
SIO_000300: 5.993e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

QD
type: SiteQuality
SIO_000300: 2.179e1

VQSLOD
type: SiteQuality
SIO_000300: -6.565e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.009e-1

GenotypeQuality
all individuals: 25276
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2828
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14412
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10123
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.083767451552407e-5
allele num: 47990
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.939e1

FS
type: SiteQuality
SIO_000300: 8.151e0

DP
type: SiteQuality
SIO_000300: 2.253282e6

QD
type: SiteQuality
SIO_000300: 1.617e1

VQSLOD
type: SiteQuality
SIO_000300: 2.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.36e-1

GenotypeQuality
all individuals: 14410
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3571
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2725
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2294
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.251172094767769e-5
allele num: 47991
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10123
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.467e-1

FS
type: SiteQuality
SIO_000300: 1.104e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-2

QD
type: SiteQuality
SIO_000300: 1.863e1

MQRankSum
type: SiteQuality
SIO_000300: 9.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.55e-1

DP
type: SiteQuality
SIO_000300: 2.253284e6

BaseQRankSum
type: SiteQuality
SIO_000300: 6.49e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

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

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

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

GenotypeQuality
all individuals: 2294
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14410
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 8079
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 1.072501072501073e-4
allele num: 9324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47993
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.877518767285657e-5
allele num: 10124
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.673e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.78e0

DP
type: SiteQuality
SIO_000300: 2.25297e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.6e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.34e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.207e0

VQSLOD
type: SiteQuality
SIO_000300: -1.316e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.72e-1

MQ
type: SiteQuality
SIO_000300: 5.99e1

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1485
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2828
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25293
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

European (Finnish)
type: Population
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allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 633
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47993
num of homozygotes: 0

African
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allele frequency: 2.34796900680911e-4
allele num: 8518
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.966e1

MQRankSum
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FS
type: SiteQuality
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BaseQRankSum
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VQSLOD
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DP
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.173984503404555e-4
allele num: 8518
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 2.083506958913243e-5
allele num: 47996
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e-1

InbreedingCoeff
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QD
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MQ
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FS
type: SiteQuality
SIO_000300: 4.15e-1

VQSLOD
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: -1.131e0

MQRankSum
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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6636
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47996
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Latino
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allele frequency: 1.072501072501073e-4
allele num: 9324
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 633
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South Asian
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MQRankSum
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ReadPosRankSum
type: SiteQuality
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QD
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BaseQRankSum
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VQSLOD
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FS
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InbreedingCoeff
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SIO_000300: 1.689e-1

ClippingRankSum
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MQ
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SIO_000300: 5.931e1

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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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 1.041731774902598e-4
allele num: 47997
num of homozygotes: 0

Other
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
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FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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SIO_000300: 5.96e1

ReadPosRankSum
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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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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 6636
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European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 47998
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African
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allele frequency: 0.0e0
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Other
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allele num: 633
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Latino
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allele frequency: 1.072501072501073e-4
allele num: 9324
num of homozygotes: 0

South Asian
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VQSLOD
type: SiteQuality
SIO_000300: -7.36e-2

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.52e-1

MQRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.788e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.398e-1

DP
type: SiteQuality
SIO_000300: 2.251724e6

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6636
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Other
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.083420142505938e-5
allele num: 47998
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9324
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 6.250130211046063e-5
allele num: 47999
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
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African
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South Asian
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allele frequency: 0.0e0
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East Asian
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Other
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allele frequency: 0.0e0
allele num: 633
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DP
type: SiteQuality
SIO_000300: 2.251524e6

BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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QD
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MQ
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InbreedingCoeff
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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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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.083376737015354e-5
allele num: 47999
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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Other
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ReadPosRankSum
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VQSLOD
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DP
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FS
type: SiteQuality
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InbreedingCoeff
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MQ
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MQRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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Other
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South Asian
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allele num: 10124
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East Asian
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Latino
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MQ
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VQSLOD
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FS
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InbreedingCoeff
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QD
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DP
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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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variant carriers: 0

European (Non-Finnish)
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South Asian
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African
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Other
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East Asian
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allele frequency: 1.506931886678722e-4
allele num: 6636
num of homozygotes: 0

European (Finnish)
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allele num: 4530
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Latino
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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BaseQRankSum
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DP
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FS
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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QD
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MQ
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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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variant carriers: 0

European (Finnish)
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European (Non-Finnish)
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allele num: 47998
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Latino
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East Asian
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African
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Other
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South Asian
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DP
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MQRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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FS
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ReadPosRankSum
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BaseQRankSum
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MQ
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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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Other
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African
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allele frequency: 2.700164357830477e-3
allele num: 8518
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East Asian
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South Asian
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Latino
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European (Non-Finnish)
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.703e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.928e-1

QD
type: SiteQuality
SIO_000300: 1.812e1

DP
type: SiteQuality
SIO_000300: 2.251071e6

MQ
type: SiteQuality
SIO_000300: 5.971e1

VQSLOD
type: SiteQuality
SIO_000300: 3.014e1

MQRankSum
type: SiteQuality
SIO_000300: -1.77e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.28e-1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1486
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.506931886678722e-4
allele num: 6636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9323
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47998
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10123
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.68e0

QD
type: SiteQuality
SIO_000300: 3.07e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.294e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.678e-1

DP
type: SiteQuality
SIO_000300: 2.247945e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.083420142505938e-5
allele num: 47998
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10123
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9323
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.249923e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.961000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.75e-1

QD
type: SiteQuality
SIO_000300: 2.072e1

VQSLOD
type: SiteQuality
SIO_000300: 5.875e1

MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 71

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 4.166840285011876e-5
allele num: 47998
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9323
num of homozygotes: 0

South Asian
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allele count: 66
allele frequency: 6.519806381507458e-3
allele num: 10123
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 6.31911532385466e-3
allele num: 633
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.971e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.65e0

MQRankSum
type: SiteQuality
SIO_000300: 2.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.961000000000001e-1

DP
type: SiteQuality
SIO_000300: 2.249923e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.875e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.34e-1

QD
type: SiteQuality
SIO_000300: 2.072e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1488
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 2
allele frequency: 2.145232221387965e-4
allele num: 9323
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47998
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10123
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.988e1

MQRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

FS
type: SiteQuality
SIO_000300: 1.521e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.924e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.91e0

VQSLOD
type: SiteQuality
SIO_000300: 9.44e-1

DP
type: SiteQuality
SIO_000300: 2.243366e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 1.361e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2727
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.878494517435543e-5
allele num: 10123
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47998
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9323
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.966e1

FS
type: SiteQuality
SIO_000300: 4.332e0

VQSLOD
type: SiteQuality
SIO_000300: 1.985e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.975e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.732e0

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 2.24312e6

QD
type: SiteQuality
SIO_000300: 2.129e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e-1

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.072616110693983e-4
allele num: 9323
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10123
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47998
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.732e0

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e-1

FS
type: SiteQuality
SIO_000300: 4.332e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

VQSLOD
type: SiteQuality
SIO_000300: 1.985e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.975e-1

DP
type: SiteQuality
SIO_000300: 2.24312e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 2.129e1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 1
allele frequency: 9.878494517435543e-5
allele num: 10123
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9323
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47997
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.863e1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.398e-1

QD
type: SiteQuality
SIO_000300: 2.882e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 23

GenotypeQuality
all individuals: 5
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47996
num of homozygotes: 0

African
type: Population
allele count: 21
allele frequency: 2.465367457149566e-3
allele num: 8518
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9323
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.013863773357444e-4
allele num: 6636
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e0

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 4.41e-1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.72e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

DP
type: SiteQuality
SIO_000300: 2.243e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

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

Latino
type: Population
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allele frequency: 0.0e0
allele num: 9323
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.167013917826485e-5
allele num: 47996
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.937e0

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.240412e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.143e-1

QD
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
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
all individuals: 2
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GenotypeQuality
all individuals: 2833
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 5
allele frequency: 5.36365586783952e-4
allele num: 9322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
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: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47994
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.697e1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 2.94e-1

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.102e0

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

DP
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.349e-1

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8517
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.083810873325137e-5
allele num: 47989
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.576e-1

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
type: SiteQuality
SIO_000300: 1.15e-1

ReadPosRankSum
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SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.405e1

DP
type: SiteQuality
SIO_000300: 2.239528e6

QD
type: SiteQuality
SIO_000300: 1.725e1

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25332
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1489
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8517
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9322
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 5.927682276229994e-4
allele num: 10122
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47989
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.05e-1

DP
type: SiteQuality
SIO_000300: 2.239528e6

VQSLOD
type: SiteQuality
SIO_000300: 1.405e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.86e0

MQRankSum
type: SiteQuality
SIO_000300: 1.15e-1

QD
type: SiteQuality
SIO_000300: 1.725e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.576e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3576
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1489
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47989
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8517
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.072731173567904e-4
allele num: 9322
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.05e-1

DP
type: SiteQuality
SIO_000300: 2.239528e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.971e1

QD
type: SiteQuality
SIO_000300: 1.725e1

MQRankSum
type: SiteQuality
SIO_000300: 1.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.576e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.86e0

VQSLOD
type: SiteQuality
SIO_000300: 1.405e1

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 6

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2830
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2726
bin: 7.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 3.21853878339234e-4
allele num: 9321
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.174122343548198e-4
allele num: 8517
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.167795444599579e-5
allele num: 47987
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.57e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.183e0

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

DP
type: SiteQuality
SIO_000300: 2.238695e6

QD
type: SiteQuality
SIO_000300: 1.76e1

VQSLOD
type: SiteQuality
SIO_000300: 2.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

FS
type: SiteQuality
SIO_000300: 3.385e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

GenotypeQuality
all individuals: 3575
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2830
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9321
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8517
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.167795444599579e-5
allele num: 47987
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.57e-1

QD
type: SiteQuality
SIO_000300: 1.76e1

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.183e0

DP
type: SiteQuality
SIO_000300: 2.238695e6

VQSLOD
type: SiteQuality
SIO_000300: 2.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

FS
type: SiteQuality
SIO_000300: 3.385e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.38e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3575
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8517
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9321
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.08389772229979e-5
allele num: 47987
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.385e0

DP
type: SiteQuality
SIO_000300: 2.238695e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.57e-1

QD
type: SiteQuality
SIO_000300: 1.76e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.183e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

GenotypeQuality
all individuals: 39
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 25346
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variant carriers: 0

GenotypeQuality
all individuals: 8093
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9320
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8517
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.08389772229979e-5
allele num: 47987
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 9.7e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

QD
type: SiteQuality
SIO_000300: 9.92e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.347e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.77e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.1e-1

DP
type: SiteQuality
SIO_000300: 2.23779e6

GenotypeQuality
all individuals: 2724
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2293
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2831
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14290
bin: 9.75e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10122
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8517
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.145922746781116e-4
allele num: 9320
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47985
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.237612e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.976e1

FS
type: SiteQuality
SIO_000300: 4.629e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.36e0

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.169794012175799e-5
allele num: 47964
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6634
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9319
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 6.49e-1

MQ
type: SiteQuality
SIO_000300: 5.93e1

DP
type: SiteQuality
SIO_000300: 2.235744e6

VQSLOD
type: SiteQuality
SIO_000300: 1.38e0

FS
type: SiteQuality
SIO_000300: 4.42e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.12e-1

QD
type: SiteQuality
SIO_000300: 1.517e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.57e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10102
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8492
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9308
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4527
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.087639088954302e-5
allele num: 47901
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 633
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.42e-2

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.226063e6

MQRankSum
type: SiteQuality
SIO_000300: 3.19e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.79e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47826
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8483
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6615
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9288
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.214337e6

MQ
type: SiteQuality
SIO_000300: 5.951e1

ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 2.098e1

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.72e-2

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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bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

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

African
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South Asian
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allele count: 11
allele frequency: 1.094636282217136e-3
allele num: 10049
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4514
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47669
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

DP
type: SiteQuality
SIO_000300: 2.172805e6

ReadPosRankSum
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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bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9273
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8426
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 47618
num of homozygotes: 0

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

East Asian
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allele count: 1
allele frequency: 1.516300227445034e-4
allele num: 6595
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4515
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

DP
type: SiteQuality
SIO_000300: 2.157738e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.15e0

QD
type: SiteQuality
SIO_000300: 8.550000000000001e0

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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bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4513
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9271
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.105130202303012e-5
allele num: 47503
num of homozygotes: 0

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

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10014
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.435e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.884e1

DP
type: SiteQuality
SIO_000300: 2.112631e6

QD
type: SiteQuality
SIO_000300: 2.953e1

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: 3

GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4510
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47437
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 3.0e-4
allele num: 10000
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
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DP
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VQSLOD
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.958e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.36e-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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variant carriers: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 625
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 6554
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
allele num: 9996
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.115148694953255e-5
allele num: 47278
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.362e0

DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -2.249e0

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: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.120665889089174e-5
allele num: 47155
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
allele num: 6552
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South 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
allele num: 4500
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.423e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.034e0

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 8.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

DP
type: SiteQuality
SIO_000300: 2.008547e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e-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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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9867
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 6440
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 617
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African
type: Population
allele count: 1
allele frequency: 1.25517760763148e-4
allele num: 7967
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4471
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.183e0

DP
type: SiteQuality
SIO_000300: 1.965628e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQ
type: SiteQuality
SIO_000300: 5.826e1

VQSLOD
type: SiteQuality
SIO_000300: -1.432e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-3

QD
type: SiteQuality
SIO_000300: 1.53e1

MQRankSum
type: SiteQuality
SIO_000300: 7.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e0

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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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9151
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7989
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.149751703678225e-5
allele num: 46517
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 615
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East Asian
type: Population
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QD
type: SiteQuality
SIO_000300: 2.18e1

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -5.01e-1

DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.928e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -9.1e-2

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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bin: 3.25e1
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Latino
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allele frequency: 0.0e0
allele num: 9102
num of homozygotes: 0

East Asian
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 2.203613926840018e-5
allele num: 45380
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4468
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African
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allele count: 2
allele frequency: 2.407318247472316e-4
allele num: 8308
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Other
type: Population
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South Asian
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allele frequency: 0.0e0
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.925e1

GenotypeQuality
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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
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European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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allele num: 9102
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East Asian
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South Asian
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Other
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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QD
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FS
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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DP
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-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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South Asian
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East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 1.099868015838099e-4
allele num: 9092
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 45350
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BaseQRankSum
type: SiteQuality
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VQSLOD
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MQRankSum
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InbreedingCoeff
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FS
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DP
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
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QD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Latino
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European (Non-Finnish)
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Other
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele num: 4479
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
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FS
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ReadPosRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.092609588741751e-4
allele num: 45762
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Latino
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allele num: 9141
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Other
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European (Finnish)
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allele frequency: 2.246686137946529e-4
allele num: 4451
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East Asian
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ClippingRankSum
type: SiteQuality
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 3.82e1

MQ
type: SiteQuality
SIO_000300: 5.85e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.37e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.517e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

QD
type: SiteQuality
SIO_000300: 1.4e-1

DP
type: SiteQuality
SIO_000300: 1.606641e6

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

GenotypeQuality
all individuals: 2423
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1185
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 5.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6295
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4488
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9155
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45966
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 577
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.496e0

VQSLOD
type: SiteQuality
SIO_000300: -3.258e0

MQRankSum
type: SiteQuality
SIO_000300: -1.18e-1

FS
type: SiteQuality
SIO_000300: 1.663e0

QD
type: SiteQuality
SIO_000300: 9.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.74e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.61e-1

DP
type: SiteQuality
SIO_000300: 1.611499e6

GenotypeQuality
all individuals: 5873
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27334
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6627
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 1.08991825613079e-4
allele num: 9175
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8360
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46171
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6453
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 580
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6551
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.46e-1

FS
type: SiteQuality
SIO_000300: 2.778e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.49e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.28e0

QD
type: SiteQuality
SIO_000300: 1.277e1

DP
type: SiteQuality
SIO_000300: 1.625487e6

MQRankSum
type: SiteQuality
SIO_000300: 1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.116e0

GenotypeQuality
all individuals: 3064
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 48
bin: 2.5e0
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GenotypeQuality
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bin: 1.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.75e1
variant carriers: 40

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2270
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 308
bin: 4.25e1
variant carriers: 2

Latino
type: Population
allele count: 1
allele frequency: 1.089561996077577e-4
allele num: 9178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.224199288256228e-4
allele num: 4496
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 44
allele frequency: 9.511456982274103e-4
allele num: 46260
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6539
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6557
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 581
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 4.776119402985075e-4
allele num: 8375
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.272e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.0e-1

QD
type: SiteQuality
SIO_000300: 1.549e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.42e0

VQSLOD
type: SiteQuality
SIO_000300: 5.79e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

DP
type: SiteQuality
SIO_000300: 1.634267e6

GenotypeQuality
all individuals: 6024
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4029
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1188
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6616
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variant carriers: 1

GenotypeQuality
all individuals: 235
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46561
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.219263204616067e-4
allele num: 4506
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6868
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8400
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9211
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.86e-1

FS
type: SiteQuality
SIO_000300: 3.257e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.22e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.029e0

MQ
type: SiteQuality
SIO_000300: 6.053e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.28e-1

QD
type: SiteQuality
SIO_000300: 2.233e1

DP
type: SiteQuality
SIO_000300: 1.652227e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.136e0

GenotypeQuality
all individuals: 6045
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 398
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variant carriers: 0

GenotypeQuality
all individuals: 279
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variant carriers: 0

GenotypeQuality
all individuals: 3095
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6616
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 29126
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.189767995240928e-4
allele num: 8405
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6992
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 589
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.288256609275499e-5
allele num: 46639
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9215
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6589
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4499
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.44e-1

QD
type: SiteQuality
SIO_000300: 1.682e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.75e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

VQSLOD
type: SiteQuality
SIO_000300: 2.86e0

DP
type: SiteQuality
SIO_000300: 1.659907e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.031e0

GenotypeQuality
all individuals: 197
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 542
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variant carriers: 0

GenotypeQuality
all individuals: 1656
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variant carriers: 0

GenotypeQuality
all individuals: 3103
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variant carriers: 0

GenotypeQuality
all individuals: 2436
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1191
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4507
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 591
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46691
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.084598698481562e-4
allele num: 9220
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7038
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.207e1

MQRankSum
type: SiteQuality
SIO_000300: 1.81e0

DP
type: SiteQuality
SIO_000300: 1.6611e6

FS
type: SiteQuality
SIO_000300: 2.068e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.36e0

VQSLOD
type: SiteQuality
SIO_000300: 3.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.113e0

GenotypeQuality
all individuals: 689
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6616
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 35
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variant carriers: 0

GenotypeQuality
all individuals: 1190
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 518
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variant carriers: 0

GenotypeQuality
all individuals: 2322
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9226
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4506
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8410
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7110
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.139266231682533e-5
allele num: 46745
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.731e0

FS
type: SiteQuality
SIO_000300: 4.167e0

DP
type: SiteQuality
SIO_000300: 1.664581e6

VQSLOD
type: SiteQuality
SIO_000300: 4.13e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

QD
type: SiteQuality
SIO_000300: 1.211e1

GenotypeQuality
all individuals: 3087
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1189
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variant carriers: 0

GenotypeQuality
all individuals: 1662
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6620
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9267
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 5.120327700972862e-4
allele num: 7812
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6613
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 603
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47156
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.694079e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.606e0

MQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.946e0

QD
type: SiteQuality
SIO_000300: 2.535e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1660
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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: 6258
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variant carriers: 0

GenotypeQuality
all individuals: 3112
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7946
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 605
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4518
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9271
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.369106846718787e-4
allele num: 8442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.117612180505262e-5
allele num: 47223
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.97e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.191e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.13e-1

QD
type: SiteQuality
SIO_000300: 2.193e1

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: -1.391e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.72e-2

FS
type: SiteQuality
SIO_000300: 9.759e0

DP
type: SiteQuality
SIO_000300: 1.698763e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.26e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2439
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variant carriers: 0

GenotypeQuality
all individuals: 500
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GenotypeQuality
all individuals: 31904
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variant carriers: 0

GenotypeQuality
all individuals: 1194
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9277
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8449
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8046
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 4.231729507849858e-5
allele num: 47262
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.87e-2

MQ
type: SiteQuality
SIO_000300: 5.948e1

DP
type: SiteQuality
SIO_000300: 1.702488e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.6e0

QD
type: SiteQuality
SIO_000300: 2.428e1

MQRankSum
type: SiteQuality
SIO_000300: 8.129999999999999e-1

FS
type: SiteQuality
SIO_000300: 9.04e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.357e0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2457
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6624
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 88
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 834
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9313
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.044932079414838e-4
allele num: 9570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.279960645579954e-5
allele num: 47771
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8508
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6635
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.32e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.25e0

FS
type: SiteQuality
SIO_000300: 6.724e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.82e-1

QD
type: SiteQuality
SIO_000300: 1.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.457e0

DP
type: SiteQuality
SIO_000300: 1.750455e6

GenotypeQuality
all individuals: 86
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2461
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1195
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6622
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 108
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9316
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8511
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 623
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.092663123090445e-5
allele num: 47786
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9635
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.52e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.052e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.85e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.79e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.49e-1

DP
type: SiteQuality
SIO_000300: 1.752556e6

FS
type: SiteQuality
SIO_000300: 7.608e0

QD
type: SiteQuality
SIO_000300: 2.009e1

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2463
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3161
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6544
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.349900129244507e-4
allele num: 8511
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4525
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9316
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9713
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47810
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.922e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.943e1

FS
type: SiteQuality
SIO_000300: 1.118e0

QD
type: SiteQuality
SIO_000300: 1.311e1

MQRankSum
type: SiteQuality
SIO_000300: 1.78e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.213e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.07e0

DP
type: SiteQuality
SIO_000300: 1.754188e6

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6423
bin: 6.75e1
variant carriers: 9

GenotypeQuality
all individuals: 3074
bin: 7.75e1
variant carriers: 13

GenotypeQuality
all individuals: 59
bin: 3.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1158
bin: 8.75e1
variant carriers: 12

GenotypeQuality
all individuals: 35195
bin: 6.25e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 1258
allele frequency: 2.630368418851671e-2
allele num: 47826
num of homozygotes: 20

European (Finnish)
type: Population
allele count: 52
allele frequency: 1.148917366327883e-2
allele num: 4526
num of homozygotes: 0

South Asian
type: Population
allele count: 74
allele frequency: 7.578084997439836e-3
allele num: 9765
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6636
num of homozygotes: 0

Latino
type: Population
allele count: 65
allele frequency: 6.976494579800365e-3
allele num: 9317
num of homozygotes: 0

Other
type: Population
allele count: 13
allele frequency: 2.07667731629393e-2
allele num: 626
num of homozygotes: 0

African
type: Population
allele count: 19
allele frequency: 2.232667450058754e-3
allele num: 8510
num of homozygotes: 0