4-184192368-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184192368
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184192368
    reference: chr 4
allele count: 1
allele frequency: 8.283219853221344e-6
allele num: 120726
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2536C>T
  hgvsp: ENSP00000384222.3:p.Gln846Ter
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2536C>T
  hgvsp: ENSP00000398577.2:p.Gln846Ter
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1928C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.4C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1582C>T
  hgvsp: ENSP00000427569.1:p.Gln528Ter
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2389C>T
  hgvsp: ENSP00000425054.1:p.Gln797Ter
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*332C>T
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14156
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7307
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2217
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4903
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 41129
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gln846Ter
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

4-184192372-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184192372
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184192372
    reference: chr 4
allele count: 4
allele frequency: 3.316309610665252e-5
allele num: 120616
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1932C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2540C>T
  hgvsp: ENSP00000398577.2:p.Pro847Leu
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1586C>T
  hgvsp: ENSP00000427569.1:p.Pro529Leu
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.8C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2540C>T
  hgvsp: ENSP00000384222.3:p.Pro847Leu
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2393C>T
  hgvsp: ENSP00000425054.1:p.Pro798Leu
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*336C>T
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7281
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6367
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1865
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Pro847Leu
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum

4-184192373-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184192373
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184192373
    reference: chr 4
allele count: 3
allele frequency: 2.487479685582568e-5
allele num: 120604
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2541G>A
  hgvsp: ENST00000448232.2:c.2541G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2394G>A
  hgvsp: ENST00000513834.1:c.2394G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2541G>A
  hgvsp: ENST00000403733.3:c.2541G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.9G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1933G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*337G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1587G>A
  hgvsp: ENST00000504005.1:c.1587G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2612
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14181
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1867
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6372
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41089
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro847Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

4-184192377-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184192377
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184192377
    reference: chr 4
allele count: 1
allele frequency: 8.299443937256203e-6
allele num: 120490
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2545G>A
  hgvsp: ENSP00000398577.2:p.Val849Ile
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.13G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1591G>A
  hgvsp: ENSP00000427569.1:p.Val531Ile
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2398G>A
  hgvsp: ENSP00000425054.1:p.Val800Ile
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2545G>A
  hgvsp: ENSP00000384222.3:p.Val849Ile
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*341G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1937G>A
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7235
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14124
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1860
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val849Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP

4-184192378-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184192378
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184192378
    reference: chr 4
allele count: 1
allele frequency: 8.311446524153063e-6
allele num: 120316
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1938T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2546T>C
  hgvsp: ENSP00000398577.2:p.Val849Ala
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.14T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1592T>C
  hgvsp: ENSP00000427569.1:p.Val531Ala
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2399T>C
  hgvsp: ENSP00000425054.1:p.Val800Ala
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2546T>C
  hgvsp: ENSP00000384222.3:p.Val849Ala
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*342T>C
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7195
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14067
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2595
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1637
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 660
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 841
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val849Ala
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum

4-184192386-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184192386
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184192386
    reference: chr 4
allele count: 54
allele frequency: 4.498800319914689e-4
allele num: 120032
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1946A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2554A>G
  hgvsp: ENSP00000384222.3:p.Ile852Val
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.22A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2554A>G
  hgvsp: ENSP00000398577.2:p.Ile852Val
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2407A>G
  hgvsp: ENSP00000425054.1:p.Ile803Val
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1600A>G
  hgvsp: ENSP00000427569.1:p.Ile534Val
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*350A>G
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7126
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2585
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 30014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13953
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4930
  bin: 9.75e1
  variant carriers: 54
genotype quality: GenotypeQuality
  all individuals: 2180
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile852Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

4-184192401-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184192401
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184192401
    reference: chr 4
allele count: 1
allele frequency: 8.411136344520145e-6
allele num: 118890
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2562+7C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1608+7C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.30+7C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*358+7C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2562+7C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1954+7C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2415+7C>T
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2136
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2154
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39133
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4887
  bin: 9.75e1
  variant carriers: 1
hgvs: c.2562+7C>T
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/4-184192402-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184192402
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184192402
    reference: chr 4
allele count: 1
allele frequency: 8.413542437908056e-6
allele num: 118856
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2562+8A>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1954+8A>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.30+8A>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*358+8A>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2415+8A>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2562+8A>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1608+8A>C
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6878
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2258
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 3.25e1
  variant carriers: 0
hgvs: c.2562+8A>C
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

4-184192413-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184192413
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184192413
    reference: chr 4
allele count: 1
allele frequency: 8.469408496510604e-6
allele num: 118072
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.30+19A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2562+19A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2562+19A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2415+19A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1608+19A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1954+19A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*358+19A>G
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12494
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1776
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3273
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 674
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2135
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

4-184192416-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184192416
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184192416
    reference: chr 4
allele count: 1
allele frequency: 8.483347189467077e-6
allele num: 117878
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1954+22A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.30+22A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*358+22A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2562+22A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1608+22A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2562+22A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2415+22A>G
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1402
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6640
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3792
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2131
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5798
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3599
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 798
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36107
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

4-184192424-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184192424
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184192424
    reference: chr 4
allele count: 6
allele frequency: 5.116398055768739e-5
allele num: 117270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.30+30G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2562+30G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2415+30G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1954+30G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*358+30G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1608+30G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2562+30G>A
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4959
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1392
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11355
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6342
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33735
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5464
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1575
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4886
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1612
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 933
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 453
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

4-184192429-GTGAAATACATATA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184192429
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184192416
    reference: chr 4
allele count: 15
allele frequency: 1.284048691126367e-4
allele num: 116818
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10511
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24326
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 950
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1603
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2083
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1671
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30892
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: GTGAAATACATATA
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

4-184192429-GTGAAATACATATATGAAATACA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184192429
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184192407
    reference: chr 4
allele count: 2
allele frequency: 1.712064921501823e-5
allele num: 116818
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 10511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1386
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24326
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2439
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2311
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 657
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30892
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4899
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4781
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1543
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
reference allele: GTGAAATACATATATGAAATACA
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

4-184192435-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184192435
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184192435
    reference: chr 4
allele count: 1
allele frequency: 8.631255502425382e-6
allele num: 115858
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2562+41T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2562+41T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1608+41T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*358+41T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1954+41T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.30+41T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2415+41T>C
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2320
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23433
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1376
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5225
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8993
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5414
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1858
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2070
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4780
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25703
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1662
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2971
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 675
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 658
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

4-184201886-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201886
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201886
    reference: chr 4
allele count: 906
allele frequency: 1.986145212206243e-2
allele num: 45616
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2563-43T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1955-43T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2416-43T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.31-43T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*359-43T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2563-43T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1609-43T>C
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 5.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3510
  bin: 2.25e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 11061
  bin: 2.5e0
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 3.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 4.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 2.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10462
  bin: 1.25e1
  variant carriers: 451
genotype depth: GenotypeDepth
  all individuals: 26255
  bin: 7.5e0
  variant carriers: 601
genotype depth: GenotypeDepth
  all individuals: 3178
  bin: 1.75e1
  variant carriers: 150
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 3.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 9.75e1
  variant carriers: 53
genotype quality: GenotypeQuality
  all individuals: 4297
  bin: 3.25e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 8.25e1
  variant carriers: 48
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 4.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 1012
  bin: 6.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 615
  bin: 5.25e1
  variant carriers: 44
genotype quality: GenotypeQuality
  all individuals: 17277
  bin: 2.25e1
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 995
  bin: 2.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 7.25e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 4865
  bin: 1.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 8062
  bin: 7.5e0
  variant carriers: 18
num of homozygotes: 14
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-184201888-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201888
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201888
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 45728
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1609-41A>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2416-41A>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*359-41A>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1955-41A>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2563-41A>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.31-41A>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2563-41A>C
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10458
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2735
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10715
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4454
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2568
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1127
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 316
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3663
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 655
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4650
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4532
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

4-184201891-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201891
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201891
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 46136
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1609-38T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.31-38T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2416-38T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*359-38T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2563-38T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2563-38T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1955-38T>C
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27146
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2228
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9958
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4012
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2477
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5159
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4455
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2261
  bin: 9.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

4-184201894-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201894
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201894
    reference: chr 4
allele count: 1
allele frequency: 2.146475487249935e-5
allele num: 46588
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2563-35A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2563-35A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.31-35A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*359-35A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1955-35A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2416-35A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1609-35A>G
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10243
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9027
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27962
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2268
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7396
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4416
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1123
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3150
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2300
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

4-184201894-ATTATG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201894
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201889
    reference: chr 4
allele count: 3
allele frequency: 6.439426461749807e-5
allele num: 46588
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2563-31_2563-27delTGTTA
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*359-31_*359-27delTGTTA
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2563-31_2563-27delTGTTA
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1955-31_*1955-27delTGTTA
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2416-31_2416-27delTGTTA
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.31-31_31-27delTGTTA
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1609-31_1609-27delTGTTA
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10243
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9027
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27962
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2291
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23450
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 404
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3150
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2300
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6017
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7396
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: ATTATG
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ

4-184201898-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201898
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201898
    reference: chr 4
allele count: 1
allele frequency: 2.11864406779661e-5
allele num: 47200
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1609-31T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*359-31T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2563-31T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2416-31T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.31-31T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1955-31T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2563-31T>C
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9651
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7527
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6649
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3660
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26118
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2269
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6467
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4161
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
population: African
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

4-184201905-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201905
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201905
    reference: chr 4
allele count: 2
allele frequency: 4.078137106969536e-5
allele num: 49042
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1955-24T>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*359-24T>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2416-24T>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2563-24T>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.31-24T>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1609-24T>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2563-24T>G
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30440
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8714
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5400
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8595
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1526
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2275
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28349
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1495
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4885
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3708
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD

4-184201908-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201908
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201908
    reference: chr 4
allele count: 1
allele frequency: 1.991397164250438e-5
allele num: 50216
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2416-21C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2563-21C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1955-21C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*359-21C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1609-21C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.31-21C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2563-21C>T
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4625
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 812
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8259
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9507
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30476
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1274
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1384
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 357
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1375
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4297
  bin: 7.5e0
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

4-184201909-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201909
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201909
    reference: chr 4
allele count: 31757
allele frequency: 4.313286067421835e-1
allele num: 73626
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2563-20G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2416-20G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*359-20G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2563-20G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1609-20G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1955-20G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.31-20G>A
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7474
  bin: 2.25e1
  variant carriers: 2591
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 2.75e1
  variant carriers: 1475
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 6838
  bin: 1.75e1
  variant carriers: 6128
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.25e1
  variant carriers: 142
genotype depth: GenotypeDepth
  all individuals: 14492
  bin: 1.25e1
  variant carriers: 10672
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.75e1
  variant carriers: 121
genotype depth: GenotypeDepth
  all individuals: 19444
  bin: 7.5e0
  variant carriers: 6650
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 4.25e1
  variant carriers: 638
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 9.75e1
  variant carriers: 1191
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 3.75e1
  variant carriers: 995
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 4.75e1
  variant carriers: 448
genotype depth: GenotypeDepth
  all individuals: 2227
  bin: 2.5e0
  variant carriers: 426
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.25e1
  variant carriers: 112
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 3.25e1
  variant carriers: 1147
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.75e1
  variant carriers: 209
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 5.25e1
  variant carriers: 316
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 8.25e1
  variant carriers: 75
genotype quality: GenotypeQuality
  all individuals: 943
  bin: 8.25e1
  variant carriers: 855
genotype quality: GenotypeQuality
  all individuals: 20313
  bin: 9.75e1
  variant carriers: 20142
genotype quality: GenotypeQuality
  all individuals: 815
  bin: 1.25e1
  variant carriers: 397
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 6.75e1
  variant carriers: 441
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 9.25e1
  variant carriers: 878
genotype quality: GenotypeQuality
  all individuals: 2242
  bin: 3.25e1
  variant carriers: 1174
genotype quality: GenotypeQuality
  all individuals: 3164
  bin: 2.5e0
  variant carriers: 138
genotype quality: GenotypeQuality
  all individuals: 1274
  bin: 1.75e1
  variant carriers: 863
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 7.25e1
  variant carriers: 455
genotype quality: GenotypeQuality
  all individuals: 897
  bin: 5.25e1
  variant carriers: 768
num of homozygotes: 5720
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

4-184201914-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201914
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201914
    reference: chr 4
allele count: 1
allele frequency: 1.472103636095981e-5
allele num: 67930
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2563-15C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*359-15C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1955-15C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2416-15C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1609-15C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2563-15C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.31-15C>T
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5513
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9605
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11082
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23758
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1876
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1997
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2327
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 208
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2267
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24837
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

4-184201930-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201930
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201930
    reference: chr 4
allele count: 2
allele frequency: 2.850302132025995e-5
allele num: 70168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2417A>T
  hgvsp: ENSP00000425054.1:p.Asp806Val
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1610A>T
  hgvsp: ENSP00000427569.1:p.Asp537Val
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2564A>T
  hgvsp: ENSP00000398577.2:p.Asp855Val
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*360A>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2564A>T
  hgvsp: ENSP00000384222.3:p.Asp855Val
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.32A>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1956A>T
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2097
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2420
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5863
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13681
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17547
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 656
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2533
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2241
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26333
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asp855Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: A
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

4-184201943-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201943
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201943
    reference: chr 4
allele count: 1
allele frequency: 1.421666192777936e-5
allele num: 70340
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1969C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.45C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2577C>T
  hgvsp: ENST00000403733.3:c.2577C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1623C>T
  hgvsp: ENST00000504005.1:c.1623C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2430C>T
  hgvsp: ENST00000513834.1:c.2430C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2577C>T
  hgvsp: ENST00000448232.2:c.2577C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*373C>T
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23428
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6182
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1819
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14432
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9426
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18508
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2111
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2044
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27157
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1780
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 775
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ala859Ala
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff

4-184201946-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201946
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201946
    reference: chr 4
allele count: 8
allele frequency: 1.141291942478886e-4
allele num: 70096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.48A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2433A>G
  hgvsp: ENST00000513834.1:c.2433A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2580A>G
  hgvsp: ENST00000403733.3:c.2580A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1972A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2580A>G
  hgvsp: ENST00000448232.2:c.2580A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1626A>G
  hgvsp: ENST00000504005.1:c.1626A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*376A>G
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14179
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1852
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1952
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6214
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9478
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23577
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 722
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1106
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 2027
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 998
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu860Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

4-184201951-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201951
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201951
    reference: chr 4
allele count: 1
allele frequency: 1.434761399179317e-5
allele num: 69698
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.53C>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2585C>G
  hgvsp: ENSP00000398577.2:p.Ala862Gly
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*381C>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2438C>G
  hgvsp: ENSP00000425054.1:p.Ala813Gly
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1977C>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2585C>G
  hgvsp: ENSP00000384222.3:p.Ala862Gly
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1631C>G
  hgvsp: ENSP00000427569.1:p.Ala544Gly
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23596
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9469
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27707
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2012
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2001
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1904
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 450
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala862Gly
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

4-184201958-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201958
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201958
    reference: chr 4
allele count: 1
allele frequency: 1.448561578352696e-5
allele num: 69034
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2592A>G
  hgvsp: ENST00000448232.2:c.2592A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2445A>G
  hgvsp: ENST00000513834.1:c.2445A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1984A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.60A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2592A>G
  hgvsp: ENST00000403733.3:c.2592A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*388A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1638A>G
  hgvsp: ENST00000504005.1:c.1638A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9779
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13297
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23975
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2028
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1996
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2043
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17766
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28738
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr864Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-184201967-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201967
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201967
    reference: chr 4
allele count: 7
allele frequency: 1.057689401952192e-4
allele num: 66182
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2601G>A
  hgvsp: ENST00000448232.2:c.2601G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1993G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1647G>A
  hgvsp: ENST00000504005.1:c.1647G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2601G>A
  hgvsp: ENST00000403733.3:c.2601G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2454G>A
  hgvsp: ENST00000513834.1:c.2454G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*397G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.69G>A
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2581
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 649
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24530
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2211
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10893
  bin: 2.25e1
  variant carriers: 3
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: 312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10702
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29421
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2090
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1002
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Glu867Glu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

4-184201970-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201970
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201970
    reference: chr 4
allele count: 1
allele frequency: 1.518925815663163e-5
allele num: 65836
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*1996G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1650G>A
  hgvsp: ENST00000504005.1:c.1650G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2604G>A
  hgvsp: ENST00000448232.2:c.2604G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*400G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.72G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2457G>A
  hgvsp: ENST00000513834.1:c.2457G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2604G>A
  hgvsp: ENST00000403733.3:c.2604G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2692
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10721
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24721
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10676
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6241
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 364
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 626
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1913
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2807
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2090
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29953
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 625
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1232
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu868Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

4-184201977-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201977
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201977
    reference: chr 4
allele count: 2
allele frequency: 3.124609423822022e-5
allele num: 64008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*407G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2611G>A
  hgvsp: ENSP00000398577.2:p.Val871Met
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.79G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2464G>A
  hgvsp: ENSP00000425054.1:p.Val822Met
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1657G>A
  hgvsp: ENSP00000427569.1:p.Val553Met
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2611G>A
  hgvsp: ENSP00000384222.3:p.Val871Met
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2003G>A
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6090
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3165
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9535
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2095
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11094
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3323
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 647
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30879
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1896
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1152
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val871Met
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ

4-184201980-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201980
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201980
    reference: chr 4
allele count: 5
allele frequency: 7.945841146743795e-5
allele num: 62926
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1660G>A
  hgvsp: ENSP00000427569.1:p.Glu554Lys
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2614G>A
  hgvsp: ENSP00000384222.3:p.Glu872Lys
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.82G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2614G>A
  hgvsp: ENSP00000398577.2:p.Glu872Lys
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2467G>A
  hgvsp: ENSP00000425054.1:p.Glu823Lys
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*410G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2006G>A
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25316
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2277
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1003
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13581
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2056
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu872Lys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

4-184201982-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201982
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201982
    reference: chr 4
allele count: 3
allele frequency: 4.808617041738796e-5
allele num: 62388
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2616A>G
  hgvsp: ENST00000403733.3:c.2616A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2469A>G
  hgvsp: ENST00000513834.1:c.2469A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1662A>G
  hgvsp: ENST00000504005.1:c.1662A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.84A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2008A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*412A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2616A>G
  hgvsp: ENST00000448232.2:c.2616A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25464
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11395
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2316
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5914
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3867
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31451
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2079
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 289
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1888
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu872Glu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/4-184201983-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201983
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201983
    reference: chr 4
allele count: 1
allele frequency: 1.633453119895459e-5
allele num: 61220
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2470C>A
  hgvsp: ENSP00000425054.1:p.Gln824Lys
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.85C>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1663C>A
  hgvsp: ENSP00000427569.1:p.Gln555Lys
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2009C>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2617C>A
  hgvsp: ENSP00000398577.2:p.Gln873Lys
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2617C>A
  hgvsp: ENSP00000384222.3:p.Gln873Lys
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*413C>A
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25474
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4015
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11548
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5801
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8002
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 647
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1031
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 843
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2065
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1870
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4259
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1678
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln873Lys
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

4-184201991-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201991
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201991
    reference: chr 4
allele count: 3
allele frequency: 5.053057099545225e-5
allele num: 59370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2017A>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*421A>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2625A>T
  hgvsp: ENSP00000384222.3:p.Leu875Phe
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1671A>T
  hgvsp: ENSP00000427569.1:p.Leu557Phe
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2625A>T
  hgvsp: ENSP00000398577.2:p.Leu875Phe
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2478A>T
  hgvsp: ENSP00000425054.1:p.Leu826Phe
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.93A>T
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11780
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5068
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1904
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11141
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2090
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5350
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 918
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu875Phe
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

4-184201995-C-CAAG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201995
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201998
    reference: chr 4
allele count: 22
allele frequency: 4.200076365024819e-4
allele num: 52380
alternate allele: CAAG
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2036_*2038dupGAA
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2644_2646dupGAA
  hgvsp: ENSP00000398577.2:p.Glu882dup
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*440_*442dupGAA
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2497_2499dupGAA
  hgvsp: ENSP00000425054.1:p.Glu833dup
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2644_2646dupGAA
  hgvsp: ENSP00000384222.3:p.Glu882dup
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1690_1692dupGAA
  hgvsp: ENSP00000427569.1:p.Glu564dup
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.112_114dupGAA
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: inframe insertion
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 6053
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24784
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12249
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6336
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1215
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu882dup
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: C
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

4-184201995-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201995
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201995
    reference: chr 4
allele count: 1
allele frequency: 1.909125620465827e-5
allele num: 52380
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2629C>G
  hgvsp: ENSP00000384222.3:p.Gln877Glu
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1675C>G
  hgvsp: ENSP00000427569.1:p.Gln559Glu
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2629C>G
  hgvsp: ENSP00000398577.2:p.Gln877Glu
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2021C>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.97C>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*425C>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2482C>G
  hgvsp: ENSP00000425054.1:p.Gln828Glu
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24784
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12249
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6053
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3845
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6336
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1257
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln877Glu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

4-184201995-CAAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201995
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201992
    reference: chr 4
allele count: 187
allele frequency: 3.570064910271096e-3
allele num: 52380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.112_114delGAA
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*440_*442delGAA
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2036_*2038delGAA
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2644_2646delGAA
  hgvsp: ENSP00000384222.3:p.Glu882del
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2497_2499delGAA
  hgvsp: ENSP00000425054.1:p.Glu833del
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1690_1692delGAA
  hgvsp: ENSP00000427569.1:p.Glu564del
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2644_2646delGAA
  hgvsp: ENSP00000398577.2:p.Glu882del
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 12249
  bin: 1.25e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 6053
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 3.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 1.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 24784
  bin: 7.5e0
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 3.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 6.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 6336
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1257
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 9.75e1
  variant carriers: 118
genotype quality: GenotypeQuality
  all individuals: 29329
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 3.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3845
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 7.75e1
  variant carriers: 6
hgvs: p.Glu882del
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: CAAG
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

4-184201995-CAAGAAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184201995
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184201989
    reference: chr 4
allele count: 1
allele frequency: 1.909125620465827e-5
allele num: 52380
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1687_1692delGAAGAA
  hgvsp: ENSP00000427569.1:p.Glu563_Glu564del
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2641_2646delGAAGAA
  hgvsp: ENSP00000398577.2:p.Glu881_Glu882del
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2641_2646delGAAGAA
  hgvsp: ENSP00000384222.3:p.Glu881_Glu882del
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2494_2499delGAAGAA
  hgvsp: ENSP00000425054.1:p.Glu832_Glu833del
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*437_*442delGAAGAA
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.109_114delGAAGAA
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 6053
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12249
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24784
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1215
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3845
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10253
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6336
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1616
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 622
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu881_Glu882del
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: CAAGAAG
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/4-184202002-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184202002
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184202002
    reference: chr 4
allele count: 1
allele frequency: 1.874414245548266e-5
allele num: 53350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2489A>C
  hgvsp: ENSP00000425054.1:p.Glu830Ala
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2028A>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2636A>C
  hgvsp: ENSP00000398577.2:p.Glu879Ala
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2636A>C
  hgvsp: ENSP00000384222.3:p.Glu879Ala
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1682A>C
  hgvsp: ENSP00000427569.1:p.Glu561Ala
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.104A>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*432A>C
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11375
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7305
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5656
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1176
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 225
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1499
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1571
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu879Ala
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

4-184202010-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184202010
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184202010
    reference: chr 4
allele count: 1
allele frequency: 2.008112775613479e-5
allele num: 49798
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2036G>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2497G>T
  hgvsp: ENSP00000425054.1:p.Glu833Ter
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1690G>T
  hgvsp: ENSP00000427569.1:p.Glu564Ter
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*440G>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2644G>T
  hgvsp: ENSP00000398577.2:p.Glu882Ter
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.112G>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2644G>T
  hgvsp: ENSP00000384222.3:p.Glu882Ter
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: stop gained
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1986
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9542
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5458
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4869
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1570
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1609
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 743
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 372
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10024
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1323
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Glu882Ter
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

4-184202017-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184202017
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184202017
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 45770
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*447G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1697G>A
  hgvsp: ENSP00000427569.1:p.Gly566Glu
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2651G>A
  hgvsp: ENSP00000384222.3:p.Gly884Glu
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2651G>A
  hgvsp: ENSP00000398577.2:p.Gly884Glu
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.119G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2504G>A
  hgvsp: ENSP00000425054.1:p.Gly835Glu
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2043G>A
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 5188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13053
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23799
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10153
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1193
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13620
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8983
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 365
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 822
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 398
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly884Glu
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/4-184202028-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184202028
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184202028
    reference: chr 4
allele count: 26
allele frequency: 6.619144602851324e-4
allele num: 39280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2515C>A
  hgvsp: ENSP00000425054.1:p.Pro839Thr
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2662C>A
  hgvsp: ENSP00000398577.2:p.Pro888Thr
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2662C>A
  hgvsp: ENSP00000384222.3:p.Pro888Thr
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1708C>A
  hgvsp: ENSP00000427569.1:p.Pro570Thr
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*458C>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2054C>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.130C>A
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 18523
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8002
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4895
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 21059
  bin: 7.5e0
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2465
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 591
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1105
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19234
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro888Thr
num of homozygotes: 2
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: DP

4-184202032-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184202032
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184202032
    reference: chr 4
allele count: 1
allele frequency: 2.605795288722118e-5
allele num: 38376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2519G>C
  hgvsp: ENSP00000425054.1:p.Arg840Thr
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*462G>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2666G>C
  hgvsp: ENSP00000398577.2:p.Arg889Thr
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1712G>C
  hgvsp: ENSP00000427569.1:p.Arg571Thr
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2666G>C
  hgvsp: ENSP00000384222.3:p.Arg889Thr
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2058G>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.134G>C
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19642
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7612
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20432
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 517
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8278
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22900
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1003
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1401
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg889Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

4-184202040-G-GGTAGAACAGAAATATA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184202040
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184202056
    reference: chr 4
allele count: 1
allele frequency: 3.136762860727729e-5
allele num: 31880
alternate allele: GGTAGAACAGAAATATA
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsp: ENSP00000384222.3:p.Asp892GlyfsTer6
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsp: ENSP00000398577.2:p.Asp892GlyfsTer6
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsp: ENSP00000425054.1:p.Asp843GlyfsTer6
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: stop_gained
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsp: ENSP00000427569.1:p.Asp574GlyfsTer6
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25937
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5278
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1722
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16407
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 309
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1086
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1280
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16457
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1121
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26524
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp892GlyfsTer6
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD

4-184202046-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184202046
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184202046
    reference: chr 4
allele count: 1
allele frequency: 3.549371761198268e-5
allele num: 28174
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2680G>A
  hgvsp: ENSP00000398577.2:p.Asp894Asn
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2680G>A
  hgvsp: ENSP00000384222.3:p.Asp894Asn
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*476G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.148G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2533G>A
  hgvsp: ENSP00000425054.1:p.Asp845Asn
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2072G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1726G>A
  hgvsp: ENSP00000427569.1:p.Asp576Asn
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4061
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14512
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28768
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1885
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1067
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp894Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

4-184202063-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184202063
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184202063
    reference: chr 4
allele count: 1
allele frequency: 4.501260352898812e-5
allele num: 22216
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2684+13T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*480+13T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2537+13T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2697T>C
  hgvsp: ENST00000448232.2:c.2697T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2076+13T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.165T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1730+13T>C
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9158
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33153
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 985
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8544
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 856
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5092
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 304
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1003
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Tyr899Tyr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

4-184202081-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184202081
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184202081
    reference: chr 4
allele count: 1
allele frequency: 5.367110347788751e-5
allele num: 18632
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2684+31G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2537+31G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1730+31G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.183G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2715G>A
  hgvsp: ENST00000448232.2:c.2715G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*480+31G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2076+31G>A
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31844
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5983
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 340
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6401
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu905Glu
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum

4-184202094-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184202094
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184202094
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 16876
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1730+44G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2076+44G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.196G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*480+44G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2537+44G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2728G>A
  hgvsp: ENSP00000398577.2:p.Val910Met
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2684+44G>A
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28042
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4728
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2730
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3351
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2208
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val910Met
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

4-184202103-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184202103
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184202103
    reference: chr 4
allele count: 1
allele frequency: 6.63129973474801e-5
allele num: 15080
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2737C>T
  hgvsp: ENSP00000398577.2:p.Arg913Trp
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.205C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2684+53C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2076+53C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2537+53C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*480+53C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1730+53C>T
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25225
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1234
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1983
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4776
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3077
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg913Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-184202104-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184202104
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184202104
    reference: chr 4
allele count: 1
allele frequency: 6.760411032990806e-5
allele num: 14792
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2076+54G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1730+54G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2537+54G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2738G>A
  hgvsp: ENSP00000398577.2:p.Arg913Gln
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2684+54G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.206G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*480+54G>A
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24528
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2229
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 2.25e1
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genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2084
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22915
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2950
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg913Gln
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD

4-184202111-AGT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184202111
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184202109
    reference: chr 4
allele count: 1
allele frequency: 7.129616426636246e-5
allele num: 14026
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2537+63_2537+64delTG
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.215_216delTG
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2747_2748delTG
  hgvsp: ENSP00000398577.2:p.Val916GlufsTer12
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2684+63_2684+64delTG
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1730+63_1730+64delTG
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2076+63_*2076+64delTG
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*480+63_*480+64delTG
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: frameshift
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23017
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1823
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 596
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4453
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1526
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val916GlufsTer12
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
reference allele: AGT
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: DP

4-184202148-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184202148
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184202148
    reference: chr 4
allele count: 10718
allele frequency: 9.752502274795268e-1
allele num: 10990
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1730+98G>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2076+98G>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2756+26G>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.250G>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2684+98G>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*480+98G>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2537+98G>T
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5727
  bin: 2.5e0
  variant carriers: 5557
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 4.75e1
  variant carriers: 123
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 3.25e1
  variant carriers: 440
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 4.25e1
  variant carriers: 177
genotype depth: GenotypeDepth
  all individuals: 1479
  bin: 1.25e1
  variant carriers: 1466
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 5.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 1.75e1
  variant carriers: 1259
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 2.75e1
  variant carriers: 661
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3927
  bin: 7.5e0
  variant carriers: 3894
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 2.25e1
  variant carriers: 966
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 3.75e1
  variant carriers: 281
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 2200
  bin: 1.75e1
  variant carriers: 2198
genotype quality: GenotypeQuality
  all individuals: 1233
  bin: 2.25e1
  variant carriers: 1226
genotype quality: GenotypeQuality
  all individuals: 3657
  bin: 7.5e0
  variant carriers: 3600
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 7.25e1
  variant carriers: 203
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 3.75e1
  variant carriers: 543
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 3.25e1
  variant carriers: 611
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 5.25e1
  variant carriers: 467
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 4.75e1
  variant carriers: 509
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 5.75e1
  variant carriers: 218
genotype quality: GenotypeQuality
  all individuals: 1113
  bin: 9.75e1
  variant carriers: 1111
num of homozygotes: 5235
population: Other
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

4-184202151-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184202151
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184202151
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 9090
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*480+101G>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2537+101G>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.253G>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1730+101G>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2076+101G>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2684+101G>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2756+29G>C
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11932
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2276
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1037
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11291
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 529
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/4-184202157-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184202157
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184202157
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 8724
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2684+107C>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2537+107C>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*480+107C>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2076+107C>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1730+107C>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151718
  ensembl transcript: ENST00000515284
  gene symbol: WWC2
  hgvsc: ENST00000515284.1:n.259C>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2756+35C>A
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2701
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11987
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1740
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 577
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1547
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2048
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10756
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

4-184203753-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184203753
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184203753
    reference: chr 4
allele count: 1
allele frequency: 8.448800270361608e-5
allele num: 11836
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2685-108C>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2538-108C>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*481-108C>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1731-108C>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2757-108C>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2077-108C>G
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3458
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20720
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3610
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12844
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 870
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 702
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-184203754-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184203754
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184203754
    reference: chr 4
allele count: 1
allele frequency: 8.330556481172943e-5
allele num: 12004
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2685-107A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2538-107A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1731-107A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*481-107A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2077-107A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2757-107A>G
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3470
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20777
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 525
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3747
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1105
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1454
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13213
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 877
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7342
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

4-184203760-T-TGAG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184203760
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184203763
    reference: chr 4
allele count: 1
allele frequency: 8.122157244964262e-5
allele num: 12312
alternate allele: TGAG
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2077-100_*2077-98dupGAG
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000420835
  ensembl transcript: ENST00000508747
  gene symbol: WWC2
  hgvsc: ENST00000508747.1:c.-32_-30dupGAG
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2757-100_2757-98dupGAG
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*481-100_*481-98dupGAG
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1731-100_1731-98dupGAG
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2685-100_2685-98dupGAG
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2538-100_2538-98dupGAG
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4405
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6278
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1407
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4032
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1280
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

4-184203799-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184203799
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184203799
    reference: chr 4
allele count: 2
allele frequency: 1.08837614279495e-4
allele num: 18376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2077-62A>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1731-62A>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2685-62A>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000420835
  ensembl transcript: ENST00000508747
  gene symbol: WWC2
  hgvsc: ENST00000508747.1:c.7A>T
  hgvsp: ENSP00000420835.1:p.Arg3Trp
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*481-62A>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2757-62A>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2538-62A>T
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30909
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5744
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5876
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28361
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 885
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg3Trp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

4-184203806-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184203806
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184203806
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 19422
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2757-55G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000420835
  ensembl transcript: ENST00000508747
  gene symbol: WWC2
  hgvsc: ENST00000508747.1:c.14G>A
  hgvsp: ENSP00000420835.1:p.Arg5His
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2538-55G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1731-55G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2685-55G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2077-55G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*481-55G>A
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32835
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6111
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4030
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 347
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30228
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 431
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3400
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6377
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 442
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg5His
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

4-184203811-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184203811
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184203811
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 19842
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2077-50C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2685-50C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*481-50C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2538-50C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000420835
  ensembl transcript: ENST00000508747
  gene symbol: WWC2
  hgvsc: ENST00000508747.1:c.19C>T
  hgvsp: ENSP00000420835.1:p.His7Tyr
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1731-50C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2757-50C>T
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33959
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2413
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3753
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His7Tyr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

4-184203815-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184203815
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184203815
    reference: chr 4
allele count: 358
allele frequency: 1.765634247386072e-2
allele num: 20276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2077-46G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2685-46G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2538-46G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000420835
  ensembl transcript: ENST00000508747
  gene symbol: WWC2
  hgvsc: ENST00000508747.1:c.23G>A
  hgvsp: ENSP00000420835.1:p.Gly8Glu
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*481-46G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2757-46G>A
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1731-46G>A
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 3.75e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 2.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 1.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 34273
  bin: 2.5e0
  variant carriers: 83
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 7.5e0
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 2.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 3.25e1
  variant carriers: 44
genotype quality: GenotypeQuality
  all individuals: 2714
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31476
  bin: 7.5e0
  variant carriers: 30
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 1.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 9.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 1062
  bin: 6.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 6457
  bin: 6.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 2.75e1
  variant carriers: 23
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 3.25e1
  variant carriers: 17
hgvs: p.Gly8Glu
num of homozygotes: 5
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

4-184203815-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184203815
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184203814
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 20276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2077-45delA
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2685-45delA
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2538-45delA
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*481-45delA
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000420835
  ensembl transcript: ENST00000508747
  gene symbol: WWC2
  hgvsc: ENST00000508747.1:c.24delA
  hgvsp: ENSP00000420835.1:p.Ala9HisfsTer16
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1731-45delA
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2757-45delA
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: frameshift
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34273
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 530
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6457
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31476
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3994
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala9HisfsTer16
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: GA
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD

4-184203818-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184203818
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184203818
    reference: chr 4
allele count: 3
allele frequency: 1.461845823993763e-4
allele num: 20522
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1731-43C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2077-43C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2685-43C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2757-43C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000420835
  ensembl transcript: ENST00000508747
  gene symbol: WWC2
  hgvsc: ENST00000508747.1:c.26C>T
  hgvsp: ENSP00000420835.1:p.Ala9Val
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*481-43C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2538-43C>T
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34786
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1102
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32299
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4417
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 820
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala9Val
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-184203829-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184203829
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184203828
    reference: chr 4
allele count: 1
allele frequency: 4.677268475210477e-5
allele num: 21380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1731-30delC
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*481-30delC
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2077-30delC
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2538-30delC
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000420835
  ensembl transcript: ENST00000508747
  gene symbol: WWC2
  hgvsc: ENST00000508747.1:c.39delC
  hgvsp: ENSP00000420835.1:p.Ser15ValfsTer10
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2685-30delC
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2757-30delC
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9125
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 34841
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1646
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 819
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 405
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1166
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7653
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 337
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser15ValfsTer10
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: AC
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ

4-184203840-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184203840
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184203840
    reference: chr 4
allele count: 0
allele frequency: 0.0e0
allele num: 22834
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2685-21T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1731-21T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2077-21T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2538-21T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*481-21T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2757-21T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000420835
  ensembl transcript: ENST00000508747
  gene symbol: WWC2
  hgvsc: ENST00000508747.1:c.48T>C
  hgvsp: ENST00000508747.1:c.48T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6891
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14794
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12090
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2039
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 286
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1215
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val16Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

4-184203841-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184203841
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184203841
    reference: chr 4
allele count: 1
allele frequency: 4.362621062734491e-5
allele num: 22922
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2077-20T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2685-20T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2757-20T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000420835
  ensembl transcript: ENST00000508747
  gene symbol: WWC2
  hgvsc: ENST00000508747.1:c.49T>C
  hgvsp: ENST00000508747.1:c.49T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2538-20T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*481-20T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1731-20T>C
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30915
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2440
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15130
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1241
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 354
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29548
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu17Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

4-184203843-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184203843
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184203843
    reference: chr 4
allele count: 1
allele frequency: 4.337265787647467e-5
allele num: 23056
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*481-18G>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2685-18G>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1731-18G>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2077-18G>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2757-18G>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000420835
  ensembl transcript: ENST00000508747
  gene symbol: WWC2
  hgvsc: ENST00000508747.1:c.51G>C
  hgvsp: ENSP00000420835.1:p.Leu17Phe
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2538-18G>C
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16057
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2457
  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: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1562
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 344
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7510
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu17Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum

4-184203857-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184203857
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184203857
    reference: chr 4
allele count: 1
allele frequency: 3.993610223642173e-5
allele num: 25040
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000420835
  ensembl transcript: ENST00000508747
  gene symbol: WWC2
  hgvsc: ENST00000508747.1:c.65A>G
  hgvsp: ENSP00000420835.1:p.His22Arg
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2685-4A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1731-4A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2538-4A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2077-4A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2757-4A>G
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*481-4A>G
  variant of: http://identifiers.org/hgnc/24148
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 911
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23641
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23063
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22879
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 988
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His22Arg
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

4-184203869-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184203869
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184203869
    reference: chr 4
allele count: 1
allele frequency: 3.682698681593872e-5
allele num: 27154
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2546T>C
  hgvsp: ENSP00000425054.1:p.Met849Thr
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000420835
  ensembl transcript: ENST00000508747
  gene symbol: WWC2
  hgvsc: ENST00000508747.1:c.77T>C
  hgvsp: ENSP00000420835.1:p.Met26Thr
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2693T>C
  hgvsp: ENSP00000384222.3:p.Met898Thr
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2765T>C
  hgvsp: ENSP00000398577.2:p.Met922Thr
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2085T>C
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1739T>C
  hgvsp: ENSP00000427569.1:p.Met580Thr
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*489T>C
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8088
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1380
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18721
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1913
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18270
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 957
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1355
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Met898Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

4-184203881-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 184203881
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 184203881
    reference: chr 4
allele count: 1
allele frequency: 3.418569670449884e-5
allele num: 29252
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000384222
  ensembl transcript: ENST00000403733
  gene symbol: WWC2
  hgvsc: ENST00000403733.3:c.2705C>T
  hgvsp: ENSP00000384222.3:p.Ala902Val
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000420835
  ensembl transcript: ENST00000508747
  gene symbol: WWC2
  hgvsc: ENST00000508747.1:c.89C>T
  hgvsp: ENSP00000420835.1:p.Ala30Val
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000427569
  ensembl transcript: ENST00000504005
  gene symbol: WWC2
  hgvsc: ENST00000504005.1:c.1751C>T
  hgvsp: ENSP00000427569.1:p.Ala584Val
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000393342
  ensembl transcript: ENST00000427431
  gene symbol: WWC2
  hgvsc: ENST00000427431.1:c.*2097C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000425054
  ensembl transcript: ENST00000513834
  gene symbol: WWC2
  hgvsc: ENST00000513834.1:c.2558C>T
  hgvsp: ENSP00000425054.1:p.Ala853Val
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000413521
  ensembl transcript: ENST00000438543
  gene symbol: WWC2
  hgvsc: ENST00000438543.1:c.*501C>T
  variant of: http://identifiers.org/hgnc/24148
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151718
  ensembl protein: ENSP00000398577
  ensembl transcript: ENST00000448232
  gene symbol: WWC2
  hgvsc: ENST00000448232.2:c.2777C>T
  hgvsp: ENSP00000398577.2:p.Ala926Val
  variant of: http://identifiers.org/hgnc/24148
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29974
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14880
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 628
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala902Val
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6391
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 663
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1645
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.112469437652811e-5
allele num: 16360
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66502
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.3e-1

FS
type: SiteQuality
SIO_000300: 3.038e0

DP
type: SiteQuality
SIO_000300: 1.736333e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.246e0

VQSLOD
type: SiteQuality
SIO_000300: -8.657e-1

MQ
type: SiteQuality
SIO_000300: 5.893e1

QD
type: SiteQuality
SIO_000300: 5.57e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.72e-1

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41065
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 574
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4903
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 958
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2213
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.140243153628883e-5
allele num: 16286
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.966955153422502e-4
allele num: 10168
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66490
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.573e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: -2.79e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.571e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.360000000000001e-1

QD
type: SiteQuality
SIO_000300: 2.02e1

DP
type: SiteQuality
SIO_000300: 1.733848e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

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

GenotypeQuality
all individuals: 2211
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4897
bin: 9.75e1
variant carriers: 3

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50407604608489e-5
allele num: 66486
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.852216748768474e-5
allele num: 10150
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.137228427642077e-5
allele num: 16294
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.626e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 9.85e0

FS
type: SiteQuality
SIO_000300: 6.666e0

DP
type: SiteQuality
SIO_000300: 1.732916e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.85e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.217e-1

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6333
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2200
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40998
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4894
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 40
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10144
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16222
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504800312998465e-5
allele num: 66454
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

QD
type: SiteQuality
SIO_000300: 1.061e1

MQ
type: SiteQuality
SIO_000300: 5.977e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.244e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.544e0

FS
type: SiteQuality
SIO_000300: 1.699e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.25e0

VQSLOD
type: SiteQuality
SIO_000300: -8.619e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-2

DP
type: SiteQuality
SIO_000300: 1.730145e6

GenotypeQuality
all individuals: 111
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1855
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 956
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2195
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6281
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4893
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 40703
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.881422924901186e-5
allele num: 10120
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16116
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66410
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.315e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.26e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

VQSLOD
type: SiteQuality
SIO_000300: -1.611e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 1.6333e1

MQRankSum
type: SiteQuality
SIO_000300: -2.62e-1

DP
type: SiteQuality
SIO_000300: 1.726824e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.49e0

GenotypeQuality
all individuals: 1631
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1093
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40577
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6246
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1841
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 49
allele frequency: 7.385079125847777e-4
allele num: 66350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15942
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.60235947258848e-4
allele num: 11528
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.922603691208574e-5
allele num: 10078
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159017153453871e-4
allele num: 8628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.04e-1

FS
type: SiteQuality
SIO_000300: 5.5e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

DP
type: SiteQuality
SIO_000300: 1.723784e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.38e-1

QD
type: SiteQuality
SIO_000300: 1.336e1

GenotypeQuality
all individuals: 952
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1800
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1623
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6041
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.006441223832528e-4
allele num: 9936
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66022
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15300
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 4.984e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.668e0

QD
type: SiteQuality
SIO_000300: 6.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.36e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -8.454e-1

DP
type: SiteQuality
SIO_000300: 1.697164e6

GenotypeQuality
all individuals: 6046
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39041
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1623
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2152
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1800
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4886
bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15284
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9932
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514921981517952e-5
allele num: 66010
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.94e-1

QD
type: SiteQuality
SIO_000300: 1.113e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.443e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e0

VQSLOD
type: SiteQuality
SIO_000300: 5.610000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.7e-2

DP
type: SiteQuality
SIO_000300: 1.694408e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.11e-1

GenotypeQuality
all individuals: 36937
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5864
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1618
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4885
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 774
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14902
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9848
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65724
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -8.175e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.099e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e0

MQ
type: SiteQuality
SIO_000300: 6.47e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

DP
type: SiteQuality
SIO_000300: 1.665385e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.47e-1

QD
type: SiteQuality
SIO_000300: 1.3e1

GenotypeQuality
all individuals: 1617
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 965
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4885
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1768
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65644
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14806
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -2.378e-1

QD
type: SiteQuality
SIO_000300: 1.403e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.61e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.79e-1

DP
type: SiteQuality
SIO_000300: 1.655121e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.44e-1

GenotypeQuality
all individuals: 1712
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 657
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2104
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4373
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1144
bin: 2.75e1
variant carriers: 0

African
type: Population
allele count: 6
allele frequency: 6.118702834998981e-4
allele num: 9806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14460
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.49e-1

QD
type: SiteQuality
SIO_000300: 1.214e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.25e-1

DP
type: SiteQuality
SIO_000300: 1.6252e6

VQSLOD
type: SiteQuality
SIO_000300: 1.86e0

FS
type: SiteQuality
SIO_000300: 4.612e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

GenotypeQuality
all individuals: 5127
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1543
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1607
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 548
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 564
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2311
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4781
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4899
bin: 9.75e1
variant carriers: 15

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532097441397273e-5
allele num: 65270
num of homozygotes: 0

South Asian
type: Population
allele count: 12
allele frequency: 8.425782895660722e-4
allele num: 14242
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.741856819369448e-4
allele num: 11482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.85e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.59e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

MQ
type: SiteQuality
SIO_000300: 5.533e1

DP
type: SiteQuality
SIO_000300: 1.596302e6

VQSLOD
type: SiteQuality
SIO_000300: 3.9e-1

FS
type: SiteQuality
SIO_000300: 1.538e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.92e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.46e-1

GenotypeQuality
all individuals: 1607
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1671
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 950
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1603
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2083
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5127
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532097441397273e-5
allele num: 65270
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.021485746383936e-5
allele num: 14242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.85e0

QD
type: SiteQuality
SIO_000300: 2.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.9e-1

DP
type: SiteQuality
SIO_000300: 1.596302e6

MQ
type: SiteQuality
SIO_000300: 5.533e1

FS
type: SiteQuality
SIO_000300: 1.538e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

GenotypeQuality
all individuals: 1607
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1646
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1305
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4879
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4705
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3344
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13756
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9716
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540404818386272e-5
allele num: 64918
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.955e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.55e0

FS
type: SiteQuality
SIO_000300: 3.052e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.76e-1

QD
type: SiteQuality
SIO_000300: 2.749e1

MQ
type: SiteQuality
SIO_000300: 5.928e1

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.12e0

DP
type: SiteQuality
SIO_000300: 1.560652e6

GenotypeQuality
all individuals: 511
bin: 7.75e1
variant carriers: 27

GenotypeQuality
all individuals: 1298
bin: 4.75e1
variant carriers: 31

GenotypeQuality
all individuals: 288
bin: 9.25e1
variant carriers: 81

GenotypeQuality
all individuals: 5849
bin: 1.75e1
variant carriers: 24

GenotypeQuality
all individuals: 2506
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3179
bin: 9.75e1
variant carriers: 980

GenotypeQuality
all individuals: 167
bin: 5.75e1
variant carriers: 48

GenotypeQuality
all individuals: 3965
bin: 6.25e1
variant carriers: 32

GenotypeQuality
all individuals: 226
bin: 8.75e1
variant carriers: 75

GenotypeQuality
all individuals: 3552
bin: 2.75e1
variant carriers: 14

Latino
type: Population
allele count: 26
allele frequency: 1.439645625692137e-2
allele num: 1806
num of homozygotes: 2

South Asian
type: Population
allele count: 31
allele frequency: 3.573075149838635e-3
allele num: 8676
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 52
allele frequency: 1.644528779253637e-2
allele num: 3162
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2808
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 760
allele frequency: 3.210272873194221e-2
allele num: 23674
num of homozygotes: 12

Other
type: Population
allele count: 6
allele frequency: 1.477832512315271e-2
allele num: 406
num of homozygotes: 0

African
type: Population
allele count: 31
allele frequency: 6.097560975609756e-3
allele num: 5084
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

DP
type: SiteQuality
SIO_000300: 7.78629e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.607e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

GenotypeQuality
all individuals: 79
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8153
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2261
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1055
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19683
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 215
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4686
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5082
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1826
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8684
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3174
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23742
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2814
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 406
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.73e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.72e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

DP
type: SiteQuality
SIO_000300: 7.80953e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 354
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21135
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7888
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3953
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 781
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1080
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3658
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 190
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23952
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8752
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2854
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.495e0

DP
type: SiteQuality
SIO_000300: 7.92134e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.62e-2

MQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

QD
type: SiteQuality
SIO_000300: 1.513e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 668
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2918
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3709
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 5.25e1
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GenotypeQuality
all individuals: 362
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23450
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6017
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 3.445899379738112e-4
allele num: 2902
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3218
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24190
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5166
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8798
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

DP
type: SiteQuality
SIO_000300: 8.052e5

BaseQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 5.475e1

MQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

QD
type: SiteQuality
SIO_000300: 1.115e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.35e-2

FS
type: SiteQuality
SIO_000300: 2.008e0

VQSLOD
type: SiteQuality
SIO_000300: 2.57e0

GenotypeQuality
all individuals: 3709
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2918
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4416
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2268
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 149
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1123
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 329
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3218
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2902
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 3.871467286101432e-4
allele num: 5166
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 5.274261603375527e-4
allele num: 1896
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.35e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

QD
type: SiteQuality
SIO_000300: 1.115e1

DP
type: SiteQuality
SIO_000300: 8.052e5

VQSLOD
type: SiteQuality
SIO_000300: 2.57e0

FS
type: SiteQuality
SIO_000300: 2.008e0

MQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

MQ
type: SiteQuality
SIO_000300: 5.475e1

GenotypeQuality
all individuals: 7331
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1930
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1943
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 452
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 199
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 24548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2962
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 5.128205128205128e-4
allele num: 1950
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 422
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8864
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5212
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-2

QD
type: SiteQuality
SIO_000300: 1.434e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.29e-2

FS
type: SiteQuality
SIO_000300: 3.143e0

DP
type: SiteQuality
SIO_000300: 8.26246e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.51e-1

GenotypeQuality
all individuals: 174
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 254
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9142
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3466
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 560
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 170
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3160
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3340
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2120
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5388
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.833307222309259e-5
allele num: 25532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9062
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.74e-1

QD
type: SiteQuality
SIO_000300: 7.18e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

DP
type: SiteQuality
SIO_000300: 8.64187e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.11e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.989000000000001e-1

GenotypeQuality
all individuals: 3313
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1041
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 258
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28857
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1235
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2285
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 10097
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3418
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.090037061260083e-4
allele num: 9174
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3406
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 446
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3288
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26154
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.17e-1

QD
type: SiteQuality
SIO_000300: 1.813e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.044e0

VQSLOD
type: SiteQuality
SIO_000300: 2.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.97e-1

DP
type: SiteQuality
SIO_000300: 8.85046e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-2

GenotypeQuality
all individuals: 1029
bin: 4.75e1
variant carriers: 899

GenotypeQuality
all individuals: 1565
bin: 3.75e1
variant carriers: 1109

GenotypeQuality
all individuals: 1861
bin: 7.5e0
variant carriers: 302

GenotypeQuality
all individuals: 6384
bin: 6.25e1
variant carriers: 515

GenotypeQuality
all individuals: 698
bin: 4.25e1
variant carriers: 551

GenotypeQuality
all individuals: 12211
bin: 2.25e1
variant carriers: 1202

GenotypeQuality
all individuals: 1870
bin: 2.75e1
variant carriers: 757

GenotypeQuality
all individuals: 821
bin: 7.75e1
variant carriers: 651

GenotypeQuality
all individuals: 955
bin: 8.75e1
variant carriers: 915

GenotypeQuality
all individuals: 607
bin: 5.75e1
variant carriers: 503

South Asian
type: Population
allele count: 3158
allele frequency: 3.006473724295506e-1
allele num: 10504
num of homozygotes: 418

European (Non-Finnish)
type: Population
allele count: 19207
allele frequency: 4.718005404077622e-1
allele num: 40710
num of homozygotes: 3664

East Asian
type: Population
allele count: 1545
allele frequency: 3.237636211232188e-1
allele num: 4772
num of homozygotes: 174

Latino
type: Population
allele count: 3208
allele frequency: 5.67787610619469e-1
allele num: 5650
num of homozygotes: 705

European (Finnish)
type: Population
allele count: 1911
allele frequency: 4.269436997319035e-1
allele num: 4476
num of homozygotes: 352

African
type: Population
allele count: 2488
allele frequency: 3.58294930875576e-1
allele num: 6944
num of homozygotes: 360

Other
type: Population
allele count: 240
allele frequency: 4.210526315789473e-1
allele num: 570
num of homozygotes: 47

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.6e-2

FS
type: SiteQuality
SIO_000300: 6.53e-1

DP
type: SiteQuality
SIO_000300: 1.144705e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.58e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.22e-1

QD
type: SiteQuality
SIO_000300: 1.834e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

VQSLOD
type: SiteQuality
SIO_000300: 4.83e0

GenotypeQuality
all individuals: 889
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2675
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 505
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13316
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1963
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1065
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3148
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37074
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.170138888888889e-4
allele num: 4608
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6656
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4160
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 546
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

MQ
type: SiteQuality
SIO_000300: 5.829e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.9e-3

FS
type: SiteQuality
SIO_000300: 3.424e0

QD
type: SiteQuality
SIO_000300: 9.52e0

VQSLOD
type: SiteQuality
SIO_000300: -1.357e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.43e-1

DP
type: SiteQuality
SIO_000300: 8.72736e5

BaseQRankSum
type: SiteQuality
SIO_000300: -2.637e0

GenotypeQuality
all individuals: 878
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1716
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1847
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 86
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 660
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2044
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4926
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4996
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.939487975174554e-4
allele num: 10312
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38228
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6922
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.443e0

DP
type: SiteQuality
SIO_000300: 9.1361e5

VQSLOD
type: SiteQuality
SIO_000300: 4.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.64e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.62e-1

QD
type: SiteQuality
SIO_000300: 1.379e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

GenotypeQuality
all individuals: 124
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2052
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1208
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 309
bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4236
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5062
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4908
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10420
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6970
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.619035147451679e-5
allele num: 38182
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.922e0

MQRankSum
type: SiteQuality
SIO_000300: -8.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.344e0

DP
type: SiteQuality
SIO_000300: 9.26771e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 5.15e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.3e-3

GenotypeQuality
all individuals: 95
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1815
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 308
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2047
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17895
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2097
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27340
bin: 2.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4234
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6936
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4884
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 2.104598547827002e-4
allele num: 38012
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5064
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.24123e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 6.08e-1

FS
type: SiteQuality
SIO_000300: 2.501e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
type: SiteQuality
SIO_000300: 9.359999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.25e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 305
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18211
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 517
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 554
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 913
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 9.75e1
variant carriers: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 572
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5048
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6922
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10396
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4182
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.649848958609359e-5
allele num: 37738
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.03e-1

FS
type: SiteQuality
SIO_000300: 4.116e0

MQRankSum
type: SiteQuality
SIO_000300: 4.03e-1

DP
type: SiteQuality
SIO_000300: 9.24613e5

VQSLOD
type: SiteQuality
SIO_000300: -1.27e0

QD
type: SiteQuality
SIO_000300: 2.294e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1948
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 840
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 509
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 437
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 415
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.680246582685607e-5
allele num: 37310
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4978
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 6886
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4112
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4816
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.984e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.87e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 9.14339e5

MQRankSum
type: SiteQuality
SIO_000300: 7.57e-1

QD
type: SiteQuality
SIO_000300: 8.789999999999999e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.14e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 2

East Asian
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allele count: 1
allele frequency: 2.114164904862579e-4
allele num: 4730
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3954
num of homozygotes: 0

South Asian
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allele count: 6
allele frequency: 5.903187721369539e-4
allele num: 10164
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 546
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 35580
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.06e-1

FS
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -2.12e-1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-3

DP
type: SiteQuality
SIO_000300: 8.85004e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.01e0

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 2.827894349867089e-5
allele num: 35362
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3934
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4498
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 538
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4714
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6650
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10140
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.092e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.35e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.057e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-3

QD
type: SiteQuality
SIO_000300: 1.001e1

MQRankSum
type: SiteQuality
SIO_000300: -2.334e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.52e-1

FS
type: SiteQuality
SIO_000300: 3.49e0

DP
type: SiteQuality
SIO_000300: 8.80353e5

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

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

African
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allele count: 1
allele frequency: 1.533742331288344e-4
allele num: 6520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10048
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
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East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4554
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 2.617801047120419e-4
allele num: 3820
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34250
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4292
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.096e0

MQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

FS
type: SiteQuality
SIO_000300: 1.102e0

DP
type: SiteQuality
SIO_000300: 8.60842e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.07e0

VQSLOD
type: SiteQuality
SIO_000300: -2.173e-1

QD
type: SiteQuality
SIO_000300: 9.93e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.932e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 124
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 177
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GenotypeQuality
all individuals: 31311
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4176
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 5.009016229212583e-4
allele num: 9982
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3748
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6426
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4450
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.32e-1

DP
type: SiteQuality
SIO_000300: 8.50112e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.000000000000001e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

QD
type: SiteQuality
SIO_000300: 9.300000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.03e0

VQSLOD
type: SiteQuality
SIO_000300: 9.9e-2

MQ
type: SiteQuality
SIO_000300: 5.969e1

MQRankSum
type: SiteQuality
SIO_000300: -8.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-1

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 9.003061040753856e-5
allele num: 33322
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6400
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9920
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4416
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3720
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.399999999999999e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.022e0

QD
type: SiteQuality
SIO_000300: 5.81e0

FS
type: SiteQuality
SIO_000300: 9.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.22e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.15e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.87e-1

DP
type: SiteQuality
SIO_000300: 8.41568e5

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 9892
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3974
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6306
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 32618
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 2.335357309668379e-4
allele num: 4282
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3652
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

MQRankSum
type: SiteQuality
SIO_000300: 1.22e0

ReadPosRankSum
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DP
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 3.145e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.1e-3

QD
type: SiteQuality
SIO_000300: 1.456e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 6124
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 4104
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 3790
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 9.514144361283775e-5
allele num: 31532
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3560
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.372e0

ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

ClippingRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 21

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: 5630
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 3354
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 3.431708991077557e-4
allele num: 2914
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.660590087122044e-5
allele num: 27318
num of homozygotes: 0

Other
type: Population
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East Asian
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allele count: 19
allele frequency: 5.388542257515599e-3
allele num: 3526
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.087429317094389e-4
allele num: 9196
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.851e0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2914
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 27318
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 3354
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African
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allele frequency: 0.0e0
allele num: 5630
num of homozygotes: 0

East Asian
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num of homozygotes: 0

South Asian
type: Population
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allele frequency: 1.087429317094389e-4
allele num: 9196
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 442
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FS
type: SiteQuality
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QD
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MQ
type: SiteQuality
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InbreedingCoeff
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SIO_000300: 7.41e-2

MQRankSum
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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SIO_000300: -5.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 8.15128e5

GenotypeQuality
all individuals: 238
bin: 8.25e1
variant carriers: 15

GenotypeQuality
all individuals: 1215
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 111
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 247
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 10253
bin: 6.25e1
variant carriers: 5

GenotypeQuality
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bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 406
bin: 7.25e1
variant carriers: 7

GenotypeQuality
all individuals: 148
bin: 9.25e1
variant carriers: 17

GenotypeQuality
all individuals: 273
bin: 5.25e1
variant carriers: 2

GenotypeQuality
all individuals: 104
bin: 8.75e1
variant carriers: 13

GenotypeQuality
all individuals: 1658
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 2
allele frequency: 4.524886877828055e-3
allele num: 442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 94
allele frequency: 3.440954681894721e-3
allele num: 27318
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 8.508224617129892e-4
allele num: 3526
num of homozygotes: 0

South Asian
type: Population
allele count: 69
allele frequency: 7.503262287951283e-3
allele num: 9196
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3354
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 3.088538091969801e-3
allele num: 2914
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 1.776198934280639e-3
allele num: 5630
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

QD
type: SiteQuality
SIO_000300: 3.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.41e-2

FS
type: SiteQuality
SIO_000300: 2.851e0

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

DP
type: SiteQuality
SIO_000300: 8.15128e5

GenotypeQuality
all individuals: 425
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1257
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29329
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
all individuals: 1629
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
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GenotypeQuality
all individuals: 238
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 247
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9196
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3354
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3526
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.660590087122044e-5
allele num: 27318
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2914
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.500000000000001e-2

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.73e-1

DP
type: SiteQuality
SIO_000300: 8.15128e5

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 2.851e0

QD
type: SiteQuality
SIO_000300: 3.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.41e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.96e-1

GenotypeQuality
all individuals: 414
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7588
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 32546
bin: 2.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1622
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variant carriers: 0

GenotypeQuality
all individuals: 818
bin: 1.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 452
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5618
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.587830080367394e-5
allele num: 27872
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9482
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3056
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3530
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3340
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.57745e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-2

FS
type: SiteQuality
SIO_000300: 1.114e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.03e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.26e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.46e0

QD
type: SiteQuality
SIO_000300: 1.359e1

GenotypeQuality
all individuals: 223
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30899
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variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
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GenotypeQuality
all individuals: 87
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GenotypeQuality
all individuals: 892
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variant carriers: 0

GenotypeQuality
all individuals: 411
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GenotypeQuality
all individuals: 9923
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GenotypeQuality
all individuals: 410
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 435
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 993
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 3.787878787878788e-4
allele num: 2640
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 25768
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3228
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 440
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.52e0

MQ
type: SiteQuality
SIO_000300: 5.82e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

VQSLOD
type: SiteQuality
SIO_000300: -2.792e0

QD
type: SiteQuality
SIO_000300: 4.0e0

DP
type: SiteQuality
SIO_000300: 7.28642e5

MQRankSum
type: SiteQuality
SIO_000300: -1.309e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.008e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.2e-2

GenotypeQuality
all individuals: 2176
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 960
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variant carriers: 0

GenotypeQuality
all individuals: 98
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GenotypeQuality
all individuals: 85
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GenotypeQuality
all individuals: 340
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variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 9.25e1
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GenotypeQuality
all individuals: 222
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variant carriers: 0

GenotypeQuality
all individuals: 28044
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variant carriers: 1

GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 1521
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4950
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2238
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3004
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8964
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 23394
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.62e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.62e-1

DP
type: SiteQuality
SIO_000300: 6.85394e5

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.67e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.72e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.223e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.846e1

GenotypeQuality
all individuals: 8199
bin: 6.25e1
variant carriers: 3

GenotypeQuality
all individuals: 22819
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 130
bin: 5.25e1
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GenotypeQuality
all individuals: 127
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 858
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1404
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variant carriers: 0

GenotypeQuality
all individuals: 92
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variant carriers: 0

GenotypeQuality
all individuals: 368
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GenotypeQuality
all individuals: 335
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
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variant carriers: 26

GenotypeQuality
all individuals: 845
bin: 2.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2674
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 17
allele frequency: 8.688541347235e-4
allele num: 19566
num of homozygotes: 1

Latino
type: Population
allele count: 2
allele frequency: 1.302083333333333e-3
allele num: 1536
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2242
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 2.263467632412856e-4
allele num: 4418
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 7.087172218284905e-4
allele num: 8466
num of homozygotes: 1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.447e1

MQRankSum
type: SiteQuality
SIO_000300: 1.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.64e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

DP
type: SiteQuality
SIO_000300: 6.28402e5

GenotypeQuality
all individuals: 766
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 796
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GenotypeQuality
all individuals: 80
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 361
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GenotypeQuality
all individuals: 20419
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GenotypeQuality
all individuals: 432
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GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8384
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.24714030853185e-5
allele num: 19058
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1440
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2616
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -2.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.17623e5

FS
type: SiteQuality
SIO_000300: 1.101e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.41e0

QD
type: SiteQuality
SIO_000300: 7.52e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.88e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

VQSLOD
type: SiteQuality
SIO_000300: -1.256e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

GenotypeQuality
all individuals: 346
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1883
bin: 1.75e1
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GenotypeQuality
all individuals: 123
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GenotypeQuality
all individuals: 86
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GenotypeQuality
all individuals: 345
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GenotypeQuality
all individuals: 428
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GenotypeQuality
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GenotypeQuality
all individuals: 50
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variant carriers: 0

GenotypeQuality
all individuals: 7473
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variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1576
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 312
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2278
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 2.585315408479835e-4
allele num: 3868
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.05e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.08e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e0

VQSLOD
type: SiteQuality
SIO_000300: 1.71e0

DP
type: SiteQuality
SIO_000300: 5.50615e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.24e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.734e0

MQ
type: SiteQuality
SIO_000300: 5.474e1

QD
type: SiteQuality
SIO_000300: 4.1e-1

GenotypeQuality
all individuals: 1556
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13507
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 9.25e1
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GenotypeQuality
all individuals: 28934
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 130
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6921
bin: 6.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.589556769884639e-5
allele num: 13176
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1260
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3556
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7128
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2080
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.741e0

MQ
type: SiteQuality
SIO_000300: 5.521e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.39e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.044e0

MQRankSum
type: SiteQuality
SIO_000300: -6.96e-1

DP
type: SiteQuality
SIO_000300: 5.12834e5

VQSLOD
type: SiteQuality
SIO_000300: -1.165e0

QD
type: SiteQuality
SIO_000300: 4.72e0

GenotypeQuality
all individuals: 74
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1805
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32590
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 422
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variant carriers: 1

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 4.75e1
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GenotypeQuality
all individuals: 256
bin: 7.25e1
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GenotypeQuality
all individuals: 100
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 3.255208333333333e-4
allele num: 3072
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10140
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5692
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1792
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 240
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.377e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.83e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.57e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 4.14877e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeQuality
all individuals: 55
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 386
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30450
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 123
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3924
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2806
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 200
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1662
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.304147465437788e-4
allele num: 4340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.69e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.674e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.340000000000001e-2

QD
type: SiteQuality
SIO_000300: 8.279999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.72e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.032e0

DP
type: SiteQuality
SIO_000300: 3.43154e5

FS
type: SiteQuality
SIO_000300: 3.757e0

MQ
type: SiteQuality
SIO_000300: 5.901e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5411
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 9.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7936
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 390
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2712
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1640
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.17e1

MQRankSum
type: SiteQuality
SIO_000300: -1.495e0

DP
type: SiteQuality
SIO_000300: 3.03297e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.35e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.092e0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 98
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23626
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2179
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 447
bin: 1.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2340
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 168
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 364
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 3.785011355034065e-4
allele num: 2642
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.33e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.457e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.27e0

MQRankSum
type: SiteQuality
SIO_000300: -1.734e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.73e1

DP
type: SiteQuality
SIO_000300: 2.76655e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.18e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.665e0

GenotypeQuality
all individuals: 294
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4596
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 109
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 254
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 417
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7266
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 4.625346901017577e-4
allele num: 2162
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 162
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1630
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.69833e5

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.44e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.89e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.57e0

MQ
type: SiteQuality
SIO_000300: 3.802e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

QD
type: SiteQuality
SIO_000300: 6.88e0

GenotypeQuality
all individuals: 36
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21865
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2768
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7018
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 6.157635467980296e-4
allele num: 1624
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1738
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 156
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2562
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.37e0

MQRankSum
type: SiteQuality
SIO_000300: 5.620000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.02e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.76e-1

FS
type: SiteQuality
SIO_000300: 2.062e0

QD
type: SiteQuality
SIO_000300: 1.946e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.92e-1

MQ
type: SiteQuality
SIO_000300: 4.752e1

DP
type: SiteQuality
SIO_000300: 2.54236e5

GenotypeQuality
all individuals: 1956
bin: 1.25e1
variant carriers: 1954

GenotypeQuality
all individuals: 160
bin: 2.5e0
variant carriers: 14

GenotypeQuality
all individuals: 404
bin: 6.25e1
variant carriers: 401

GenotypeQuality
all individuals: 218
bin: 8.25e1
variant carriers: 218

GenotypeQuality
all individuals: 244
bin: 4.25e1
variant carriers: 244

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

GenotypeQuality
all individuals: 356
bin: 6.75e1
variant carriers: 356

GenotypeQuality
all individuals: 216
bin: 9.25e1
variant carriers: 216

GenotypeQuality
all individuals: 436
bin: 2.75e1
variant carriers: 432

GenotypeQuality
all individuals: 108
bin: 8.75e1
variant carriers: 108

Other
type: Population
allele count: 128
allele frequency: 1.0e0
allele num: 128
num of homozygotes: 64

European (Finnish)
type: Population
allele count: 1612
allele frequency: 1.0e0
allele num: 1612
num of homozygotes: 806

African
type: Population
allele count: 1909
allele frequency: 8.797235023041474e-1
allele num: 2170
num of homozygotes: 836

Latino
type: Population
allele count: 296
allele frequency: 9.932885906040269e-1
allele num: 298
num of homozygotes: 147

East Asian
type: Population
allele count: 502
allele frequency: 1.0e0
allele num: 502
num of homozygotes: 251

European (Non-Finnish)
type: Population
allele count: 5761
allele frequency: 9.984402079722704e-1
allele num: 5770
num of homozygotes: 2876

South Asian
type: Population
allele count: 510
allele frequency: 1.0e0
allele num: 510
num of homozygotes: 255

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.906e-1

DP
type: SiteQuality
SIO_000300: 1.84465e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.94e-1

QD
type: SiteQuality
SIO_000300: 3.429e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

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

GenotypeQuality
all individuals: 887
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 105
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variant carriers: 0

GenotypeQuality
all individuals: 562
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variant carriers: 0

GenotypeQuality
all individuals: 711
bin: 1.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 398
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 122
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 452
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1674
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4654
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1532
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.05e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.965e1

VQSLOD
type: SiteQuality
SIO_000300: 3.05e-1

DP
type: SiteQuality
SIO_000300: 1.44735e5

GenotypeQuality
all individuals: 45
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 143
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 4.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 442
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1528
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4416
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 262
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.39443e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 3.44e1

VQSLOD
type: SiteQuality
SIO_000300: -1.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.23e-2

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
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variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 1.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 360
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.242144177449168e-4
allele num: 1082
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4494
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1024
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4500
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.81e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.165e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 8.539999999999999e0

DP
type: SiteQuality
SIO_000300: 1.69903e5

BaseQRankSum
type: SiteQuality
SIO_000300: 7.1e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.226e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.5e-2

GenotypeQuality
all individuals: 44
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 663
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variant carriers: 0

GenotypeQuality
all individuals: 878
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 8.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 364
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1090
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 224
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.189141856392294e-4
allele num: 4568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4576
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1028
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.770000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.71679e5

MQRankSum
type: SiteQuality
SIO_000300: -1.102e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.168e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

VQSLOD
type: SiteQuality
SIO_000300: -2.508e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.528e0

QD
type: SiteQuality
SIO_000300: 7.16e0

GenotypeQuality
all individuals: 111
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 98
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1054
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1142
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 366
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 232
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 2.131287297527707e-4
allele num: 4692
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4668
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.36e0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e0

DP
type: SiteQuality
SIO_000300: 1.8021e5

MQRankSum
type: SiteQuality
SIO_000300: -1.171e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.09e-1

QD
type: SiteQuality
SIO_000300: 2.496e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.57e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.549e1

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3254
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 458
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1472
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 222
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6940
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1670
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.729257641921397e-4
allele num: 7328
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.42e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.99917e5

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -4.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.834e0

QD
type: SiteQuality
SIO_000300: 1.111e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 2472
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 125
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variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 230
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 478
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7588
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7448
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1830
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.28e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 3.22274e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.45e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.231e0

VQSLOD
type: SiteQuality
SIO_000300: -2.96e0

GenotypeQuality
all individuals: 6525
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 482
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31413
bin: 7.5e0
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GenotypeQuality
all individuals: 231
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1046
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7666
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1562
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1918
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7654
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 494
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.43e-1

FS
type: SiteQuality
SIO_000300: 6.73e-1

QD
type: SiteQuality
SIO_000300: 1.624e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

VQSLOD
type: SiteQuality
SIO_000300: -1.304e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.34315e5

GenotypeQuality
all individuals: 363
bin: 7.25e1
variant carriers: 13

GenotypeQuality
all individuals: 545
bin: 1.25e1
variant carriers: 15

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 87
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variant carriers: 6

GenotypeQuality
all individuals: 117
bin: 8.75e1
variant carriers: 13

GenotypeQuality
all individuals: 3994
bin: 2.25e1
variant carriers: 14

GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 530
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variant carriers: 378

GenotypeQuality
all individuals: 117
bin: 3.75e1
variant carriers: 5

GenotypeQuality
all individuals: 276
bin: 8.25e1
variant carriers: 3

Other
type: Population
allele count: 9
allele frequency: 3.71900826446281e-2
allele num: 242
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 4.995004995004995e-3
allele num: 2002
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 113
allele frequency: 1.43765903307888e-2
allele num: 7860
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 27
allele frequency: 1.693851944792974e-2
allele num: 1594
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 6.134969325153374e-3
allele num: 326
num of homozygotes: 0

South Asian
type: Population
allele count: 197
allele frequency: 2.546535677352637e-2
allele num: 7736
num of homozygotes: 3

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 516
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.84e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 3.51323e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.54e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.509e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 242
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1062
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variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2002
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 326
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7860
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1594
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7736
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.84e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.84e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.54e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.0e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.51323e5

QD
type: SiteQuality
SIO_000300: 1.509e1

GenotypeQuality
all individuals: 228
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 122
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GenotypeQuality
all individuals: 65
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variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.288992008249549e-4
allele num: 7758
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 328
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2096
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 242
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.507522567703109e-4
allele num: 7976
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1600
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.153e1

DP
type: SiteQuality
SIO_000300: 3.57142e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.190000000000001e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.54e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.237e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7844
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.181474480151229e-4
allele num: 8464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2278
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1634
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 556
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 358
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.49e0

MQRankSum
type: SiteQuality
SIO_000300: 7.32e-1

DP
type: SiteQuality
SIO_000300: 3.94831e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.122e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.72e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.65e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.02e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
all individuals: 50
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9320
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7890
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1672
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.65e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 4.43431e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 4.608e0

MQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

QD
type: SiteQuality
SIO_000300: 1.834e1

MQ
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -7.88e-1

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 337
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
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GenotypeQuality
all individuals: 61
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GenotypeQuality
all individuals: 48
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GenotypeQuality
all individuals: 7420
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GenotypeQuality
all individuals: 151
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GenotypeQuality
all individuals: 12579
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GenotypeQuality
all individuals: 435
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variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.066098081023454e-4
allele num: 9380
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1674
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7890
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 416
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.26e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

QD
type: SiteQuality
SIO_000300: 1.987e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.36e-1

FS
type: SiteQuality
SIO_000300: 2.745e0

MQRankSum
type: SiteQuality
SIO_000300: -3.61e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.78e-1

DP
type: SiteQuality
SIO_000300: 4.4621e5

GenotypeQuality
all individuals: 1145
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1244
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 983
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28932
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13706
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.056635672020287e-4
allele num: 9464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2658
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1680
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 256
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7894
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.76e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.98e-1

QD
type: SiteQuality
SIO_000300: 1.582e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.51e-2

VQSLOD
type: SiteQuality
SIO_000300: -6.845e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 4.53788e5

ClippingRankSum
type: SiteQuality
SIO_000300: 3.25e-1

GenotypeQuality
all individuals: 20395
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1303
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1965
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 8073
bin: 6.25e1
variant carriers: 2

GenotypeQuality
all individuals: 533
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 143
bin: 8.75e1
variant carriers: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3030
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7940
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1766
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.923076923076923e-3
allele num: 520
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10664
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.24e-2

DP
type: SiteQuality
SIO_000300: 5.10559e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.231e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 5.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.597e-1

GenotypeQuality
all individuals: 8614
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 159
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24822
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 543
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 549
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1012
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12044
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3316
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.607717041800643e-3
allele num: 622
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 276
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1866
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.332e0

VQSLOD
type: SiteQuality
SIO_000300: -1.458e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.39e-2

QD
type: SiteQuality
SIO_000300: 6.41e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

DP
type: SiteQuality
SIO_000300: 5.51664e5