7-73097973-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73097973
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73097973
    reference: chr 7
allele count: 2
allele frequency: 2.162910412250725e-5
allele num: 92468
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+260G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.47G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.18G>A
  hgvsp: ENST00000428163.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.18G>A
  hgvsp: ENST00000436944.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.18G>A
  hgvsp: ENST00000421744.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.18G>A
  hgvsp: ENST00000423497.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.18G>A
  hgvsp: ENST00000265758.2:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.18G>A
  hgvsp: ENST00000441822.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.18G>A
  hgvsp: ENST00000432522.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.-11G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.18G>A
  hgvsp: ENST00000421304.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.35G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.47G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.18G>A
  hgvsp: ENST00000430270.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.13G>A
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12781
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8391
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg6Arg
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum

7-73097974-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73097974
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73097974
    reference: chr 7
allele count: 1
allele frequency: 1.069953564015322e-5
allele num: 93462
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.19C>T
  hgvsp: ENSP00000390136.1:p.Arg7Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.-10C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.19C>T
  hgvsp: ENSP00000404981.1:p.Arg7Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.19C>T
  hgvsp: ENSP00000392039.1:p.Arg7Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.19C>T
  hgvsp: ENSP00000391410.1:p.Arg7Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.48C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.48C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.14C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.19C>T
  hgvsp: ENSP00000390048.1:p.Arg7Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.19C>T
  hgvsp: ENSP00000265758.2:p.Arg7Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+261C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.19C>T
  hgvsp: ENSP00000401191.1:p.Arg7Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.36C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.19C>T
  hgvsp: ENSP00000398314.1:p.Arg7Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.19C>T
  hgvsp: ENSP00000391761.1:p.Arg7Cys
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12265
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27211
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg7Cys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

7-73097975-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73097975
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73097975
    reference: chr 7
allele count: 1
allele frequency: 1.04982467927856e-5
allele num: 95254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.20G>T
  hgvsp: ENSP00000390048.1:p.Arg7Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.20G>T
  hgvsp: ENSP00000391410.1:p.Arg7Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.20G>T
  hgvsp: ENSP00000398314.1:p.Arg7Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.20G>T
  hgvsp: ENSP00000401191.1:p.Arg7Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.37G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.15G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.-9G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.20G>T
  hgvsp: ENSP00000392039.1:p.Arg7Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.49G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.20G>T
  hgvsp: ENSP00000265758.2:p.Arg7Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.49G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.20G>T
  hgvsp: ENSP00000404981.1:p.Arg7Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.20G>T
  hgvsp: ENSP00000390136.1:p.Arg7Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.20G>T
  hgvsp: ENSP00000391761.1:p.Arg7Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+262G>T
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11549
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg7Leu
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

7-73097978-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73097978
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73097978
    reference: chr 7
allele count: 3
allele frequency: 3.078249091916518e-5
allele num: 97458
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.52C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.23C>T
  hgvsp: ENSP00000404981.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.23C>T
  hgvsp: ENSP00000401191.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.23C>T
  hgvsp: ENSP00000392039.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.40C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.18C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.23C>T
  hgvsp: ENSP00000390136.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.23C>T
  hgvsp: ENSP00000265758.2:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.23C>T
  hgvsp: ENSP00000390048.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+265C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.23C>T
  hgvsp: ENSP00000391410.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.52C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.23C>T
  hgvsp: ENSP00000391761.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.-6C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.23C>T
  hgvsp: ENSP00000398314.1:p.Pro8Leu
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1985
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9307
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro8Leu
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

7-73097983-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73097983
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73097983
    reference: chr 7
allele count: 1
allele frequency: 9.837484751898635e-6
allele num: 101652
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.28C>T
  hgvsp: ENSP00000398314.1:p.His10Tyr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.23C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.28C>T
  hgvsp: ENSP00000390048.1:p.His10Tyr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+270C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.45C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.28C>T
  hgvsp: ENSP00000391761.1:p.His10Tyr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.28C>T
  hgvsp: ENSP00000391410.1:p.His10Tyr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.28C>T
  hgvsp: ENSP00000392039.1:p.His10Tyr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.28C>T
  hgvsp: ENSP00000390136.1:p.His10Tyr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.28C>T
  hgvsp: ENSP00000404981.1:p.His10Tyr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.28C>T
  hgvsp: ENSP00000401191.1:p.His10Tyr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.57C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.57C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.-1C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.28C>T
  hgvsp: ENSP00000265758.2:p.His10Tyr
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10171
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His10Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum

7-73097986-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73097986
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73097986
    reference: chr 7
allele count: 10
allele frequency: 9.655678504528513e-5
allele num: 103566
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+273G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.26G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.31G>A
  hgvsp: ENSP00000265758.2:p.Gly11Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: start_lost
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.3G>A
  hgvsp: ENSP00000397056.2:p.Met1?
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.31G>A
  hgvsp: ENSP00000398314.1:p.Gly11Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.31G>A
  hgvsp: ENSP00000390136.1:p.Gly11Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.31G>A
  hgvsp: ENSP00000391761.1:p.Gly11Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.31G>A
  hgvsp: ENSP00000401191.1:p.Gly11Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.48G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.31G>A
  hgvsp: ENSP00000390048.1:p.Gly11Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.31G>A
  hgvsp: ENSP00000391410.1:p.Gly11Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.31G>A
  hgvsp: ENSP00000392039.1:p.Gly11Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.60G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.31G>A
  hgvsp: ENSP00000404981.1:p.Gly11Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.60G>A
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: start lost
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3687
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2210
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10539
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7841
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met1?
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum

7-73097989-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73097989
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73097989
    reference: chr 7
allele count: 1
allele frequency: 9.501368197020371e-6
allele num: 105248
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.34G>A
  hgvsp: ENSP00000392039.1:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.34G>A
  hgvsp: ENSP00000391761.1:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.34G>A
  hgvsp: ENSP00000390048.1:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.34G>A
  hgvsp: ENSP00000390136.1:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.34G>A
  hgvsp: ENSP00000265758.2:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.29G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.34G>A
  hgvsp: ENSP00000404981.1:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.51G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.34G>A
  hgvsp: ENSP00000391410.1:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+276G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.34G>A
  hgvsp: ENSP00000401191.1:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.34G>A
  hgvsp: ENSP00000398314.1:p.Gly12Arg
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.6G>A
  hgvsp: ENST00000423166.2:c.6G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.63G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.63G>A
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1457
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33651
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly12Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

7-73097994-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73097994
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73097994
    reference: chr 7
allele count: 1
allele frequency: 9.289363678588016e-6
allele num: 107650
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.34C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.39C>T
  hgvsp: ENST00000430270.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.39C>T
  hgvsp: ENST00000436944.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.11C>T
  hgvsp: ENSP00000397056.2:p.Pro4Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+281C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.39C>T
  hgvsp: ENST00000423497.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.39C>T
  hgvsp: ENST00000265758.2:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.56C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.39C>T
  hgvsp: ENST00000441822.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.39C>T
  hgvsp: ENST00000432522.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.68C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.68C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.39C>T
  hgvsp: ENST00000428163.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.39C>T
  hgvsp: ENST00000421304.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.39C>T
  hgvsp: ENST00000421744.1:c.39C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12415
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6087
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro4Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

7-73097995-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73097995
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73097995
    reference: chr 7
allele count: 1
allele frequency: 9.259430730198708e-6
allele num: 107998
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.40C>T
  hgvsp: ENSP00000392039.1:p.Pro14Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.35C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.12C>T
  hgvsp: ENST00000423166.2:c.12C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.57C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.40C>T
  hgvsp: ENSP00000265758.2:p.Pro14Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.69C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.40C>T
  hgvsp: ENSP00000401191.1:p.Pro14Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.40C>T
  hgvsp: ENSP00000390136.1:p.Pro14Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+282C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.40C>T
  hgvsp: ENSP00000391410.1:p.Pro14Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.40C>T
  hgvsp: ENSP00000391761.1:p.Pro14Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.40C>T
  hgvsp: ENSP00000404981.1:p.Pro14Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.40C>T
  hgvsp: ENSP00000390048.1:p.Pro14Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.40C>T
  hgvsp: ENSP00000398314.1:p.Pro14Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.69C>T
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2804
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12558
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5943
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro14Ser
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

7-73098001-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098001
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098001
    reference: chr 7
allele count: 1
allele frequency: 9.083807205275875e-6
allele num: 110086
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.46C>G
  hgvsp: ENSP00000390048.1:p.Leu16Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.46C>G
  hgvsp: ENSP00000404981.1:p.Leu16Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.46C>G
  hgvsp: ENSP00000265758.2:p.Leu16Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.46C>G
  hgvsp: ENSP00000398314.1:p.Leu16Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.46C>G
  hgvsp: ENSP00000401191.1:p.Leu16Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.46C>G
  hgvsp: ENSP00000390136.1:p.Leu16Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.46C>G
  hgvsp: ENSP00000391410.1:p.Leu16Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.46C>G
  hgvsp: ENSP00000391761.1:p.Leu16Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.63C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.46C>G
  hgvsp: ENSP00000392039.1:p.Leu16Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.18C>G
  hgvsp: ENSP00000397056.2:p.Ser6Arg
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.41C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.75C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+288C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.75C>G
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2375
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13325
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu16Val
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD

7-73098008-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098008
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098008
    reference: chr 7
allele count: 1
allele frequency: 8.905671131376461e-6
allele num: 112288
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.48+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.48+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.65+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+295G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.48+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.77+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.48+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.43+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.77+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.48+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.48+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.48+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.20+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.48+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.48+5G>A
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1972
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.48+5G>A
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

7-73098012-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098012
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098012
    reference: chr 7
allele count: 1
allele frequency: 8.844235327413593e-6
allele num: 113068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.48+9C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.48+9C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.48+9C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.20+9C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+299C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.77+9C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.43+9C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.48+9C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.48+9C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.65+9C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.77+9C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.48+9C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.48+9C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.48+9C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.48+9C>T
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3066
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
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: C
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

7-73098018-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098018
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098018
    reference: chr 7
allele count: 10
allele frequency: 8.696105883785241e-5
allele num: 114994
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.48+15C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.48+15C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.43+15C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.48+15C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.48+15C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.48+15C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.77+15C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.48+15C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.77+15C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.48+15C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.20+15C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.48+15C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+305C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.65+15C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.48+15C>T
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35406
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
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: C
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

7-73098019-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098019
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098019
    reference: chr 7
allele count: 489
allele frequency: 4.239859885202975e-3
allele num: 115334
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.77+16C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.48+16C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.43+16C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+306C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.48+16C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.48+16C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.65+16C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.77+16C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.20+16C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.48+16C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.48+16C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.48+16C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.48+16C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.48+16C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.48+16C>G
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 3.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 3.25e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 7.5e0
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 35339
  bin: 2.25e1
  variant carriers: 41
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 16224
  bin: 2.75e1
  variant carriers: 65
genotype quality: GenotypeQuality
num of homozygotes: 15
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/7-73098024-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098024
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098024
    reference: chr 7
allele count: 1
allele frequency: 8.538105565137207e-6
allele num: 117122
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.43+21A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.48+21A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.20+21A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.77+21A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.48+21A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.48+21A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.48+21A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.77+21A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.48+21A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.48+21A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.48+21A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+311A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.48+21A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.65+21A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.48+21A>C
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/7-73098028-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098028
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098028
    reference: chr 7
allele count: 2
allele frequency: 1.693853007436015e-5
allele num: 118074
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.77+25C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.48+25C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.48+25C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.48+25C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+315C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.48+25C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.43+25C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.48+25C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.20+25C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.77+25C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.48+25C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.48+25C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.48+25C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.65+25C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.48+25C>A
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17500
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 1
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

7-73098028-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098028
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098028
    reference: chr 7
allele count: 1
allele frequency: 8.469265037180074e-6
allele num: 118074
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.48+25C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.48+25C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+315C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.48+25C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.48+25C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.48+25C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.48+25C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.20+25C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.77+25C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.48+25C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.43+25C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.65+25C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.77+25C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.48+25C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.48+25C>T
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17500
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

7-73098035-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098035
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098035
    reference: chr 7
allele count: 2
allele frequency: 1.679120141046092e-5
allele num: 119110
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.48+32C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.65+32C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.48+32C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.48+32C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.48+32C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.48+32C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.77+32C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.48+32C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.48+32C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.20+32C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+322C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.48+32C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.77+32C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.48+32C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.43+32C>T
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36666
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1077
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18044
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

7-73098045-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098045
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098045
    reference: chr 7
allele count: 1
allele frequency: 8.332083520805212e-6
allele num: 120018
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.48+42C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.77+42C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.77+42C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.48+42C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.48+42C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+332C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.43+42C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.48+42C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.48+42C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.48+42C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.65+42C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.48+42C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.48+42C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.20+42C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.48+42C>T
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3517
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-73098049-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098049
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098049
    reference: chr 7
allele count: 1
allele frequency: 8.306337735692333e-6
allele num: 120390
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.77+46C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.48+46C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.48+46C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.20+46C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.48+46C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.43+46C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.48+46C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+336C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.48+46C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.48+46C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.77+46C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.48+46C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.48+46C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.48+46C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.65+46C>T
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

7-73098050-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098050
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098050
    reference: chr 7
allele count: 1
allele frequency: 8.302200083022e-6
allele num: 120450
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.77+47A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.43+47A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.48+47A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.65+47A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.20+47A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.48+47A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.48+47A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.48+47A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.48+47A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.48+47A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+337A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.48+47A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.77+47A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.48+47A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.48+47A>G
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

7-73098055-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098055
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098055
    reference: chr 7
allele count: 1
allele frequency: 8.283357078956959e-6
allele num: 120724
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+342G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.49-42G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.49-42G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.66-42G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.49-42G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.78-42G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.78-42G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.49-42G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.49-42G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.49-42G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.21-42G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.49-42G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.49-42G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.44-42G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.49-42G>A
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18739
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum

7-73098059-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098059
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098059
    reference: chr 7
allele count: 1
allele frequency: 8.273762245168123e-6
allele num: 120864
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.44-38G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.78-38G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.49-38G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.49-38G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.49-38G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+346G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.66-38G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.49-38G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.21-38G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.78-38G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.49-38G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.49-38G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.49-38G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.49-38G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.49-38G>A
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37430
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

7-73098064-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098064
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098064
    reference: chr 7
allele count: 18
allele frequency: 1.487480373522849e-4
allele num: 121010
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.49-33A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.78-33A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.78-33A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.49-33A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.44-33A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+351A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.49-33A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.49-33A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.49-33A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.49-33A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.49-33A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.49-33A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.66-33A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.49-33A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.21-33A>G
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37474
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

7-73098068-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098068
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098068
    reference: chr 7
allele count: 4
allele frequency: 3.30436506625252e-5
allele num: 121052
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.49-29C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.49-29C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.44-29C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.78-29C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.66-29C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.49-29C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.49-29C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.21-29C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.78-29C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.49-29C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.49-29C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.49-29C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+355C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.49-29C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.49-29C>T
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18841
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff

7-73098070-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098070
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098070
    reference: chr 7
allele count: 1
allele frequency: 8.259275166011431e-6
allele num: 121076
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.49-27C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.78-27C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.49-27C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.66-27C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.21-27C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.49-27C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.49-27C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.44-27C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.49-27C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+357C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.49-27C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.49-27C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.49-27C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.49-27C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.78-27C>T
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18850
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37481
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

7-73098073-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098073
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098073
    reference: chr 7
allele count: 1
allele frequency: 8.257638315441784e-6
allele num: 121100
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.78-24C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.49-24C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.21-24C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.49-24C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.49-24C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.49-24C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.49-24C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+360C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.78-24C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.66-24C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.44-24C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.49-24C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.49-24C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.49-24C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.49-24C>G
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD

7-73098074-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098074
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098074
    reference: chr 7
allele count: 2
allele frequency: 1.651418568550385e-5
allele num: 121108
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.49-23A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.78-23A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.49-23A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.49-23A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.49-23A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.21-23A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.49-23A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.49-23A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.44-23A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.78-23A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+361A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.49-23A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.49-23A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.49-23A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.66-23A>G
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37504
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

7-73098077-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098077
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098077
    reference: chr 7
allele count: 2
allele frequency: 1.651173158529135e-5
allele num: 121126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.66-20C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.44-20C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.49-20C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.49-20C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.49-20C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.49-20C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.78-20C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.78-20C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.21-20C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+364C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.49-20C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.49-20C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.49-20C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.49-20C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.49-20C>T
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

7-73098079-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098079
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098079
    reference: chr 7
allele count: 16
allele frequency: 1.320894906299018e-4
allele num: 121130
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.49-18A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.49-18A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.49-18A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.49-18A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.44-18A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.49-18A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.49-18A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.49-18A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.78-18A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+366A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.21-18A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.49-18A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.78-18A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.66-18A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.49-18A>G
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18866
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3612
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

7-73098082-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098082
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098082
    reference: chr 7
allele count: 4
allele frequency: 3.301964668978042e-5
allele num: 121140
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.49-15T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.78-15T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.49-15T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.49-15T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.21-15T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.49-15T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.66-15T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.49-15T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.49-15T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.44-15T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.49-15T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+369T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.78-15T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.49-15T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.49-15T>C
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18880
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37510
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

7-73098098-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098098
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098098
    reference: chr 7
allele count: 1
allele frequency: 8.255320554097116e-6
allele num: 121134
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.50T>C
  hgvsp: ENSP00000401191.1:p.Phe17Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.50T>C
  hgvsp: ENSP00000265758.2:p.Phe17Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.50T>C
  hgvsp: ENSP00000398314.1:p.Phe17Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.45T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.22T>C
  hgvsp: ENSP00000397056.2:p.Phe8Leu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.50T>C
  hgvsp: ENSP00000392039.1:p.Phe17Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.50T>C
  hgvsp: ENSP00000391410.1:p.Phe17Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.50T>C
  hgvsp: ENSP00000390136.1:p.Phe17Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.50T>C
  hgvsp: ENSP00000404981.1:p.Phe17Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.79T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.50T>C
  hgvsp: ENSP00000390048.1:p.Phe17Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+385T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.79T>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.50T>C
  hgvsp: ENSP00000391761.1:p.Phe17Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.67T>C
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe17Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

7-73098107-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098107
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098107
    reference: chr 7
allele count: 1
allele frequency: 8.256683785524381e-6
allele num: 121114
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.59A>T
  hgvsp: ENSP00000401191.1:p.Glu20Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+394A>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.59A>T
  hgvsp: ENSP00000398314.1:p.Glu20Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.31A>T
  hgvsp: ENSP00000397056.2:p.Arg11Ter
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.59A>T
  hgvsp: ENSP00000390048.1:p.Glu20Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.59A>T
  hgvsp: ENSP00000391761.1:p.Glu20Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.59A>T
  hgvsp: ENSP00000265758.2:p.Glu20Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.59A>T
  hgvsp: ENSP00000404981.1:p.Glu20Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.59A>T
  hgvsp: ENSP00000392039.1:p.Glu20Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.88A>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.59A>T
  hgvsp: ENSP00000390136.1:p.Glu20Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.76A>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.59A>T
  hgvsp: ENSP00000391410.1:p.Glu20Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.88A>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.54A>T
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg11Ter
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-73098113-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098113
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098113
    reference: chr 7
allele count: 2
allele frequency: 1.651827747402501e-5
allele num: 121078
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.65A>G
  hgvsp: ENSP00000265758.2:p.Glu22Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.37A>G
  hgvsp: ENSP00000397056.2:p.Lys13Glu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.94A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+400A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.65A>G
  hgvsp: ENSP00000401191.1:p.Glu22Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.65A>G
  hgvsp: ENSP00000391761.1:p.Glu22Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.82A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.65A>G
  hgvsp: ENSP00000398314.1:p.Glu22Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.65A>G
  hgvsp: ENSP00000391410.1:p.Glu22Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.65A>G
  hgvsp: ENSP00000390048.1:p.Glu22Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.65A>G
  hgvsp: ENSP00000390136.1:p.Glu22Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.65A>G
  hgvsp: ENSP00000404981.1:p.Glu22Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.65A>G
  hgvsp: ENSP00000392039.1:p.Glu22Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.94A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.60A>G
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18878
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37390
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu22Gly
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

7-73098114-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098114
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098114
    reference: chr 7
allele count: 2
allele frequency: 1.651827747402501e-5
allele num: 121078
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.95A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.66A>G
  hgvsp: ENST00000421744.1:c.66A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.66A>G
  hgvsp: ENST00000441822.1:c.66A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.66A>G
  hgvsp: ENST00000421304.1:c.66A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.95A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.61A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.66A>G
  hgvsp: ENST00000265758.2:c.66A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.66A>G
  hgvsp: ENST00000436944.1:c.66A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.38A>G
  hgvsp: ENSP00000397056.2:p.Lys13Arg
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.66A>G
  hgvsp: ENST00000423497.1:c.66A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.66A>G
  hgvsp: ENST00000432522.1:c.66A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+401A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.66A>G
  hgvsp: ENST00000428163.1:c.66A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.83A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.66A>G
  hgvsp: ENST00000430270.1:c.66A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37389
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys13Arg
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum

7-73098115-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098115
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098115
    reference: chr 7
allele count: 1
allele frequency: 8.260093834665961e-6
allele num: 121064
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.67G>A
  hgvsp: ENSP00000390048.1:p.Ala23Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.67G>A
  hgvsp: ENSP00000391761.1:p.Ala23Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.96G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.67G>A
  hgvsp: ENSP00000392039.1:p.Ala23Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.67G>A
  hgvsp: ENSP00000390136.1:p.Ala23Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.67G>A
  hgvsp: ENSP00000401191.1:p.Ala23Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.62G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.67G>A
  hgvsp: ENSP00000404981.1:p.Ala23Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.67G>A
  hgvsp: ENSP00000398314.1:p.Ala23Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.67G>A
  hgvsp: ENSP00000265758.2:p.Ala23Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.84G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.67G>A
  hgvsp: ENSP00000391410.1:p.Ala23Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.96G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+402G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.39G>A
  hgvsp: ENST00000423166.2:c.39G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37375
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala23Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS

7-73098116-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098116
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098116
    reference: chr 7
allele count: 1
allele frequency: 8.261868173631421e-6
allele num: 121038
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.63C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+403C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.68C>T
  hgvsp: ENSP00000391410.1:p.Ala23Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.68C>T
  hgvsp: ENSP00000392039.1:p.Ala23Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.68C>T
  hgvsp: ENSP00000390048.1:p.Ala23Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.68C>T
  hgvsp: ENSP00000398314.1:p.Ala23Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.97C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.68C>T
  hgvsp: ENSP00000391761.1:p.Ala23Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.68C>T
  hgvsp: ENSP00000401191.1:p.Ala23Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.68C>T
  hgvsp: ENSP00000265758.2:p.Ala23Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.68C>T
  hgvsp: ENSP00000404981.1:p.Ala23Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.68C>T
  hgvsp: ENSP00000390136.1:p.Ala23Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.40C>T
  hgvsp: ENSP00000397056.2:p.Pro14Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.85C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.97C>T
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18883
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37359
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala23Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

7-73098118-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098118
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098118
    reference: chr 7
allele count: 1
allele frequency: 8.261868173631421e-6
allele num: 121038
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.70C>G
  hgvsp: ENSP00000398314.1:p.Arg24Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.65C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.70C>G
  hgvsp: ENSP00000391410.1:p.Arg24Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.70C>G
  hgvsp: ENSP00000391761.1:p.Arg24Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.70C>G
  hgvsp: ENSP00000401191.1:p.Arg24Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.99C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+405C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.70C>G
  hgvsp: ENSP00000390136.1:p.Arg24Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.70C>G
  hgvsp: ENSP00000392039.1:p.Arg24Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.70C>G
  hgvsp: ENSP00000404981.1:p.Arg24Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.42C>G
  hgvsp: ENST00000423166.2:c.42C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.70C>G
  hgvsp: ENSP00000390048.1:p.Arg24Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.87C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.99C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.70C>G
  hgvsp: ENSP00000265758.2:p.Arg24Gly
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37349
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg24Gly
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: DP

7-73098119-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098119
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098119
    reference: chr 7
allele count: 20
allele frequency: 1.652564780539397e-4
allele num: 121024
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.71G>A
  hgvsp: ENSP00000401191.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+406G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.66G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.71G>A
  hgvsp: ENSP00000392039.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.88G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.71G>A
  hgvsp: ENSP00000404981.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.71G>A
  hgvsp: ENSP00000391410.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.71G>A
  hgvsp: ENSP00000390136.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.71G>A
  hgvsp: ENSP00000398314.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.43G>A
  hgvsp: ENSP00000397056.2:p.Gly15Arg
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.71G>A
  hgvsp: ENSP00000390048.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.71G>A
  hgvsp: ENSP00000391761.1:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.71G>A
  hgvsp: ENSP00000265758.2:p.Arg24Gln
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.100G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.100G>A
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg24Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

7-73098125-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098125
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098125
    reference: chr 7
allele count: 1
allele frequency: 8.266922390132602e-6
allele num: 120964
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.106A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.77A>G
  hgvsp: ENSP00000390136.1:p.Tyr26Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.77A>G
  hgvsp: ENSP00000392039.1:p.Tyr26Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.72A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.94A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.77A>G
  hgvsp: ENSP00000391410.1:p.Tyr26Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.77A>G
  hgvsp: ENSP00000401191.1:p.Tyr26Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.106A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.77A>G
  hgvsp: ENSP00000404981.1:p.Tyr26Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.77A>G
  hgvsp: ENSP00000265758.2:p.Tyr26Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.77A>G
  hgvsp: ENSP00000391761.1:p.Tyr26Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.77A>G
  hgvsp: ENSP00000390048.1:p.Tyr26Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.49A>G
  hgvsp: ENSP00000397056.2:p.Thr17Ala
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+412A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.77A>G
  hgvsp: ENSP00000398314.1:p.Tyr26Cys
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr26Cys
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: DP

7-73098130-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098130
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098130
    reference: chr 7
allele count: 2
allele frequency: 1.654095540558423e-5
allele num: 120912
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.82C>T
  hgvsp: ENSP00000404981.1:p.Arg28Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.82C>T
  hgvsp: ENSP00000401191.1:p.Arg28Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.82C>T
  hgvsp: ENSP00000390048.1:p.Arg28Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.82C>T
  hgvsp: ENSP00000391761.1:p.Arg28Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.82C>T
  hgvsp: ENSP00000392039.1:p.Arg28Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.99C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.82C>T
  hgvsp: ENSP00000265758.2:p.Arg28Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.111C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.82C>T
  hgvsp: ENSP00000390136.1:p.Arg28Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.77C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.82C>T
  hgvsp: ENSP00000391410.1:p.Arg28Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.82C>T
  hgvsp: ENSP00000398314.1:p.Arg28Cys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+417C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.111C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.54C>T
  hgvsp: ENST00000423166.2:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg28Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
reference allele: C
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/7-73098134-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098134
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098134
    reference: chr 7
allele count: 1
allele frequency: 8.275268532463878e-6
allele num: 120842
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86A>C
  hgvsp: ENSP00000390048.1:p.Asn29Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.86A>C
  hgvsp: ENSP00000391410.1:p.Lys29Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86A>C
  hgvsp: ENSP00000401191.1:p.Asn29Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.86A>C
  hgvsp: ENSP00000392039.1:p.Lys29Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86A>C
  hgvsp: ENSP00000265758.2:p.Asn29Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.86A>C
  hgvsp: ENSP00000391761.1:p.Lys29Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+421A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86A>C
  hgvsp: ENSP00000390136.1:p.Asn29Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.86A>C
  hgvsp: ENSP00000398314.1:p.Lys29Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115A>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86A>C
  hgvsp: ENSP00000404981.1:p.Asn29Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.58A>C
  hgvsp: ENSP00000397056.2:p.Ser20Arg
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn29Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

7-73098134-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098134
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098133
    reference: chr 7
allele count: 1
allele frequency: 8.275268532463878e-6
allele num: 120842
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+1delG
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+422delG
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+1delG
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+1delG
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.87delG
  hgvsp: ENSP00000398314.1:p.Lys29AsnfsTer49
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+1delG
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+1delG
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.59delG
  hgvsp: ENSP00000397056.2:p.Ser20MetfsTer5
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+1delG
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+1delG
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+1delG
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+1delG
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.87delG
  hgvsp: ENSP00000391761.1:p.Lys29AsnfsTer45
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.87delG
  hgvsp: ENSP00000392039.1:p.Lys29AsnfsTer?
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.87delG
  hgvsp: ENSP00000391410.1:p.Lys29AsnfsTer105
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.86+1delG
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: AG
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: VQSLOD

7-73098137-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098137
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098137
    reference: chr 7
allele count: 20
allele frequency: 1.656150113446283e-4
allele num: 120762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+3G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+3G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+3G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+3G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.89G>A
  hgvsp: ENST00000436944.1:c.89G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+3G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+424G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+3G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.89G>A
  hgvsp: ENST00000430270.1:c.89G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.89G>A
  hgvsp: ENST00000441822.1:c.89G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.61G>A
  hgvsp: ENSP00000397056.2:p.Glu21Lys
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+3G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.89G>A
  hgvsp: ENST00000421304.1:c.89G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+3G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+3G>A
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3624
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu21Lys
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

7-73098139-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098139
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098139
    reference: chr 7
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.63G>A
  hgvsp: ENST00000423166.2:c.63G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*1G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*1G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+426G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*1G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*1G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+5G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+5G>A
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.86+5G>A
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: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum

7-73098141-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098141
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098141
    reference: chr 7
allele count: 1
allele frequency: 8.283768783445716e-6
allele num: 120718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+7G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+7G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+7G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+7G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+428G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*3G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*3G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+7G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+7G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*3G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*3G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+7G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.65G>A
  hgvsp: ENSP00000397056.2:p.Gly22Glu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+7G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+7G>A
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly22Glu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQ

7-73098142-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098142
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098142
    reference: chr 7
allele count: 3
allele frequency: 2.486119167978785e-5
allele num: 120670
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+8G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+8G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*4G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+8G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+8G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*4G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+8G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+8G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+8G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+8G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*4G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.66G>T
  hgvsp: ENST00000423166.2:c.66G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*4G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+8G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+429G>T
  variant of: http://identifiers.org/hgnc/16405
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.86+8G>T
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

7-73098148-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098148
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098148
    reference: chr 7
allele count: 1
allele frequency: 8.305509875251242e-6
allele num: 120402
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+14G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*10G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*10G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+14G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+435G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+14G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.72G>C
  hgvsp: ENST00000423166.2:c.72G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+14G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+14G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*10G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+14G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+14G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*10G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+14G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+14G>C
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu24Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

7-73098155-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098155
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098155
    reference: chr 7
allele count: 1
allele frequency: 8.318221896887321e-6
allele num: 120218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+21G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+442G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*17G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+21G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+21G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+21G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+21G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*17G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*17G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+21G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+21G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.79G>A
  hgvsp: ENSP00000397056.2:p.Ala27Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*17G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+21G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+21G>A
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala27Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum

http://identifiers.org/exac.variant/7-73098156-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098156
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098156
    reference: chr 7
allele count: 5
allele frequency: 4.164861893179622e-5
allele num: 120052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*18C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+22C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+22C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+22C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*18C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+22C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.80C>A
  hgvsp: ENSP00000397056.2:p.Ala27Glu
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+22C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*18C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+22C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+443C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+22C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*18C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+22C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+22C>A
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3585
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36669
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Ala27Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ

7-73098157-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098157
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098157
    reference: chr 7
allele count: 1
allele frequency: 8.33152816889674e-6
allele num: 120026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+23G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.81G>C
  hgvsp: ENST00000423166.2:c.81G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+23G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*19G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*19G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*19G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+23G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+444G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+23G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*19G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+23G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+23G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+23G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+23G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+23G>C
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala27Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

7-73098162-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098162
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098162
    reference: chr 7
allele count: 7
allele frequency: 5.836543432221055e-5
allele num: 119934
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+28G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+28G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+28G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+28G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+28G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+449G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+28G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.86G>A
  hgvsp: ENSP00000397056.2:p.Arg29His
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+28G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+28G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+28G>A
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 18503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36660
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg29His
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP

7-73098179-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098179
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098179
    reference: chr 7
allele count: 1
allele frequency: 8.378156470450242e-6
allele num: 119358
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+45C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+45C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*41C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*41C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+466C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+45C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.103C>G
  hgvsp: ENSP00000397056.2:p.Arg35Gly
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*41C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+45C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+45C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+45C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+45C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*41C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+45C>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+45C>G
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18254
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 715
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg35Gly
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum

7-73098180-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098180
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098180
    reference: chr 7
allele count: 1
allele frequency: 8.378296859814337e-6
allele num: 119356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+46G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*42G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+46G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+46G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*42G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+46G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+46G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+46G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+467G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.104G>A
  hgvsp: ENSP00000397056.2:p.Arg35Gln
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*42G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+46G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*42G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+46G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+46G>A
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3430
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg35Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum

7-73098184-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098184
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098184
    reference: chr 7
allele count: 1
allele frequency: 8.396869646995599e-6
allele num: 119092
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+50A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+50A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*46A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+50A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+50A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+50A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*46A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.108A>G
  hgvsp: ENST00000423166.2:c.108A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+471A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*46A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*46A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+50A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+50A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+50A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+50A>G
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36303
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln36Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

7-73098188-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098188
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098188
    reference: chr 7
allele count: 1
allele frequency: 8.420059950826851e-6
allele num: 118764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*50G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*50G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*50G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+54G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+54G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*50G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+54G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.112G>A
  hgvsp: ENSP00000397056.2:p.Ala38Thr
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+54G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+54G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+475G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+54G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+54G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+54G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+54G>A
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18095
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala38Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

7-73098190-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098190
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098190
    reference: chr 7
allele count: 13
allele frequency: 1.095419461390677e-4
allele num: 118676
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+56C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.114C>T
  hgvsp: ENST00000423166.2:c.114C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*52C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*52C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+56C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*52C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*52C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+56C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+56C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+56C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+56C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+56C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+56C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+56C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+477C>T
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18054
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3364
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 3.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Ala38Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: MQ

7-73098191-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098191
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098191
    reference: chr 7
allele count: 3
allele frequency: 2.529638936202506e-5
allele num: 118594
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*53C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.115C>T
  hgvsp: ENSP00000397056.2:p.Pro39Ser
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*53C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+57C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*53C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*53C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+57C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+57C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+57C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+57C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+57C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+57C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+57C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+57C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+478C>T
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18026
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3353
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro39Ser
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ

7-73098198-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098198
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098198
    reference: chr 7
allele count: 3
allele frequency: 2.548506575146964e-5
allele num: 117716
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+64C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+64C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+485C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*60C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+64C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*60C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+64C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+64C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*60C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*60C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+64C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+64C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.122C>T
  hgvsp: ENSP00000397056.2:p.Ala41Val
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+64C>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+64C>T
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala41Val
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD

7-73098214-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098214
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098214
    reference: chr 7
allele count: 2
allele frequency: 1.738193321861257e-5
allele num: 115062
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+80A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*76A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.138A>G
  hgvsp: ENST00000423166.2:c.138A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+80A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+80A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*76A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+80A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+80A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+80A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+80A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+80A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*76A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*76A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+501A>G
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+80A>G
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16390
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys46Lys
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS

7-73098232-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098232
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098232
    reference: chr 7
allele count: 1
allele frequency: 9.086778736937755e-6
allele num: 110050
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+519G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+98G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+98G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+98G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+98G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+98G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+98G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+98G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*93+1G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+98G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*93+1G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*94G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.155+1G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+98G>T
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*94G>T
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14292
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30483
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*93+1G>T
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

7-73098247-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098247
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098248
    reference: chr 7
allele count: 2
allele frequency: 1.960438354015958e-5
allele num: 102018
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+113_86+114insC
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+113_103+114insC
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+113_81+114insC
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+113_86+114insC
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+113_115+114insC
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*93+16_*93+17insC
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*109_*110insC
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*109_*110insC
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*93+16_*93+17insC
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+113_115+114insC
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+113_86+114insC
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.155+16_155+17insC
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+113_86+114insC
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+113_86+114insC
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+534_359+535insC
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6642
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2303
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22388
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10586
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

http://identifiers.org/exac.variant/7-73098251-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098251
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098251
    reference: chr 7
allele count: 3
allele frequency: 3.011020334423992e-5
allele num: 99634
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+117C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*93+20C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*113C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*113C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+117C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+117C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+117C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+117C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+117C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+117C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+117C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.155+20C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*93+20C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+117C>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+538C>A
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2743
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15592
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.*113C>A
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

7-73098253-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098253
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098253
    reference: chr 7
allele count: 5
allele frequency: 5.068115471942913e-5
allele num: 98656
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000496153
  gene symbol: WBSCR22
  hgvsc: ENST00000496153.1:n.115+119G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000392039
  ensembl transcript: ENST00000441822
  gene symbol: WBSCR22
  hgvsc: ENST00000441822.1:c.*93+22G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391761
  ensembl transcript: ENST00000421304
  gene symbol: WBSCR22
  hgvsc: ENST00000421304.1:c.*115G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000404981
  ensembl transcript: ENST00000421744
  gene symbol: WBSCR22
  hgvsc: ENST00000421744.1:c.86+119G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000397056
  ensembl transcript: ENST00000423166
  gene symbol: WBSCR22
  hgvsc: ENST00000423166.2:c.155+22G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000265758
  ensembl transcript: ENST00000265758
  gene symbol: WBSCR22
  hgvsc: ENST00000265758.2:c.86+119G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000463307
  gene symbol: WBSCR22
  hgvsc: ENST00000463307.1:n.103+119G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000487006
  gene symbol: WBSCR22
  hgvsc: ENST00000487006.1:n.81+119G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000398314
  ensembl transcript: ENST00000430270
  gene symbol: WBSCR22
  hgvsc: ENST00000430270.1:c.*115G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000391410
  ensembl transcript: ENST00000436944
  gene symbol: WBSCR22
  hgvsc: ENST00000436944.1:c.*93+22G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000401191
  ensembl transcript: ENST00000423497
  gene symbol: WBSCR22
  hgvsc: ENST00000423497.1:c.86+119G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+119G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390136
  ensembl transcript: ENST00000432522
  gene symbol: WBSCR22
  hgvsc: ENST00000432522.1:c.86+119G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000478670
  gene symbol: WBSCR22
  hgvsc: ENST00000478670.1:n.115+119G>A
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+540G>A
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2950
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17862
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7467
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4915
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.*115G>A
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

7-73098254-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 73098254
    reference: chr 7
  end: Position
    type: ExactPosition
    position: 73098254
    reference: chr 7
allele count: 1
allele frequency: 1.012371175767883e-5
allele num: 98778
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl transcript: ENST00000464615
  gene symbol: WBSCR22
  hgvsc: ENST00000464615.1:n.359+541G>C
  variant of: http://identifiers.org/hgnc/16405
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000071462
  ensembl protein: ENSP00000390048
  ensembl transcript: ENST00000428163
  gene symbol: WBSCR22
  hgvsc: ENST00000428163.1:c.86+120G>C
  variant of: http://identifiers.org/hgnc/16405
canonical: false
consequence: splice donor
filter: PASS
hgvs: c.*115+1G>C
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 10
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1331
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 224
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6811
bin: 1.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26431
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31159
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 666
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1353
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2244
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2876
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 2.754062241806665e-4
allele num: 7262
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Latino
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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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South Asian
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VQSLOD
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MQ
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DP
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ClippingRankSum
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QD
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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FS
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
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European (Finnish)
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East Asian
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South Asian
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African
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European (Non-Finnish)
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Other
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BaseQRankSum
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DP
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ReadPosRankSum
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QD
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VQSLOD
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MQRankSum
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FS
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InbreedingCoeff
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MQ
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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Latino
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East Asian
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European (Non-Finnish)
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European (Finnish)
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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QD
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DP
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FS
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BaseQRankSum
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MQRankSum
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SIO_000300: -4.1e-2

ReadPosRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele num: 9398
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Other
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European (Finnish)
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African
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South Asian
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East Asian
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European (Non-Finnish)
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ReadPosRankSum
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DP
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VQSLOD
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MQRankSum
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MQ
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FS
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BaseQRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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South Asian
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European (Non-Finnish)
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African
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East Asian
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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MQ
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VQSLOD
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QD
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InbreedingCoeff
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FS
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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African
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Latino
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South Asian
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MQRankSum
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MQ
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QD
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DP
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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FS
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele frequency: 1.754940156540662e-5
allele num: 56982
num of homozygotes: 0

European (Finnish)
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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

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

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

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

MQRankSum
type: SiteQuality
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FS
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SIO_000300: 1.549e0

ReadPosRankSum
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DP
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: -3.1e-3

VQSLOD
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MQ
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SIO_000300: 5.889e1

QD
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

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

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

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

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

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

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

African
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allele count: 1
allele frequency: 1.211240310077519e-4
allele num: 8256
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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DP
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SIO_000300: 1.283749e6

ReadPosRankSum
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ClippingRankSum
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MQ
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QD
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VQSLOD
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InbreedingCoeff
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SIO_000300: -2.0e-3

MQRankSum
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SIO_000300: -2.95e-1

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -1.616e0

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8282
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 58564
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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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: 1
allele frequency: 1.25344697919278e-4
allele num: 7978
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.75e-1

QD
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SIO_000300: 1.746e1

ReadPosRankSum
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SIO_000300: 5.95e-1

VQSLOD
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FS
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.288355e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.027e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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
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num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8080
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.672296732332185e-5
allele num: 59798
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 5.949e1

DP
type: SiteQuality
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ClippingRankSum
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SIO_000300: -6.32e-1

FS
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QD
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BaseQRankSum
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SIO_000300: -2.87e-1

InbreedingCoeff
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SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

MQRankSum
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SIO_000300: 2.87e-1

VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

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

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 61060
num of homozygotes: 0

European (Finnish)
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Other
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MQRankSum
type: SiteQuality
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VQSLOD
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MQ
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InbreedingCoeff
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ClippingRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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DP
type: SiteQuality
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QD
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GenotypeDepth
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variant carriers: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.626703972411101e-5
allele num: 61474
num of homozygotes: 0

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

Latino
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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South Asian
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Other
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BaseQRankSum
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SIO_000300: 3.34e-1

DP
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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FS
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QD
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MQ
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 7.97702616464582e-4
allele num: 6268
num of homozygotes: 0

African
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Other
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East Asian
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European (Non-Finnish)
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allele num: 62734
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South Asian
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Latino
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MQ
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FS
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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QD
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MQRankSum
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InbreedingCoeff
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 1.199616122840691e-4
allele num: 8336
num of homozygotes: 0

Other
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European (Non-Finnish)
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allele frequency: 9.537434430138292e-5
allele num: 62910
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South Asian
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African
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allele num: 9272
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Latino
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allele frequency: 1.156789464317494e-3
allele num: 11238
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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MQ
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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DP
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FS
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MQRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 8414
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African
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allele frequency: 0.0e0
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
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BaseQRankSum
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DP
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ClippingRankSum
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FS
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MQ
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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QD
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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allele num: 16470
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Latino
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num of homozygotes: 0

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

European (Non-Finnish)
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African
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East Asian
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Latino
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European (Finnish)
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Other
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BaseQRankSum
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FS
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DP
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VQSLOD
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MQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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InbreedingCoeff
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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Other
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South Asian
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East Asian
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European (Non-Finnish)
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African
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DP
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ClippingRankSum
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MQ
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BaseQRankSum
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MQRankSum
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QD
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FS
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Non-Finnish)
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African
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East Asian
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Latino
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European (Finnish)
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FS
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VQSLOD
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QD
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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MQ
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ReadPosRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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South Asian
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Other
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European (Non-Finnish)
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Latino
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ReadPosRankSum
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DP
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ClippingRankSum
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FS
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InbreedingCoeff
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VQSLOD
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QD
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BaseQRankSum
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MQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele num: 6592
num of homozygotes: 0

South Asian
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African
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East Asian
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Latino
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num of homozygotes: 0

Other
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European (Non-Finnish)
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
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DP
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InbreedingCoeff
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ClippingRankSum
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MQ
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66402
num of homozygotes: 0

Other
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Latino
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East Asian
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African
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South Asian
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European (Finnish)
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FS
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QD
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ClippingRankSum
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InbreedingCoeff
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DP
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VQSLOD
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ReadPosRankSum
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MQRankSum
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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European (Finnish)
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South Asian
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Other
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ReadPosRankSum
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VQSLOD
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MQRankSum
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FS
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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South Asian
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European (Non-Finnish)
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Latino
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East Asian
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FS
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ReadPosRankSum
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DP
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MQRankSum
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BaseQRankSum
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QD
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MQ
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

Latino
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allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

African
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num of homozygotes: 0

South Asian
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allele frequency: 1.211387038158692e-4
allele num: 16510
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500870504892838e-5
allele num: 66628
num of homozygotes: 0

African
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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DP
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InbreedingCoeff
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BaseQRankSum
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FS
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ClippingRankSum
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MQ
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QD
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MQRankSum
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

South Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.000930288389401e-5
allele num: 66646
num of homozygotes: 0

Other
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East Asian
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allele count: 0
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African
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Latino
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European (Finnish)
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South Asian
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FS
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VQSLOD
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MQRankSum
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DP
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MQ
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InbreedingCoeff
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ClippingRankSum
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QD
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

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

European (Finnish)
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South Asian
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African
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Other
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DP
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ClippingRankSum
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MQ
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MQRankSum
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ReadPosRankSum
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VQSLOD
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FS
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InbreedingCoeff
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BaseQRankSum
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QD
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GenotypeDepth
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variant carriers: 0

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

European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.510437120502674e-5
allele num: 66206
num of homozygotes: 0

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

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

European (Finnish)
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num of homozygotes: 0

European (Non-Finnish)
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Latino
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South Asian
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Other
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African
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East Asian
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ReadPosRankSum
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FS
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InbreedingCoeff
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ClippingRankSum
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MQ
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MQRankSum
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DP
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VQSLOD
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QD
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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African
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European (Non-Finnish)
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Latino
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South Asian
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FS
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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QD
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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East Asian
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African
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European (Non-Finnish)
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ClippingRankSum
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QD
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FS
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VQSLOD
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MQ
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BaseQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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African
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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InbreedingCoeff
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ReadPosRankSum
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FS
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BaseQRankSum
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MQ
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MQRankSum
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DP
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VQSLOD
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
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African
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East Asian
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Latino
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South Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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QD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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FS
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BaseQRankSum
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DP
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MQ
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ClippingRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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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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European (Non-Finnish)
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allele num: 65348
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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South Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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ReadPosRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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DP
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QD
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FS
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MQ
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variant carriers: 0

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

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

Latino
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East Asian
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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DP
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SIO_000300: 1.27189e6

QD
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MQ
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VQSLOD
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MQRankSum
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ClippingRankSum
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FS
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele num: 13392
num of homozygotes: 0

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

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

Latino
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East Asian
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MQRankSum
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SIO_000300: 1.59e0

DP
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SIO_000300: 1.106686e6

FS
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SIO_000300: 0.0e0

BaseQRankSum
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QD
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ClippingRankSum
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SIO_000300: 6.6e-1

VQSLOD
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.5e-3

MQ
type: SiteQuality
SIO_000300: 5.97e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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Other
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European (Non-Finnish)
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African
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European (Finnish)
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Latino
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ClippingRankSum
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QD
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FS
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VQSLOD
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MQ
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
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South Asian
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East Asian
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Other
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Latino
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European (Finnish)
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QD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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VQSLOD
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DP
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FS
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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