8-28321120-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321120
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321120
    reference: chr 8
allele count: 9
allele frequency: 7.658922644881286e-5
allele num: 117510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000520481
  gene symbol: FBXO16
  hgvsc: ENST00000520481.1:n.54+9A>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.222+9A>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.284+9A>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.342+9A>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.306+9A>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.306+9A>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.342+9A>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.342+9A>T
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13738
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4046
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1235
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33661
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5347
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2383
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39848
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 1388
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1745
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

8-28321122-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321122
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321122
    reference: chr 8
allele count: 1
allele frequency: 8.49516625040352e-6
allele num: 117714
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000520481
  gene symbol: FBXO16
  hgvsc: ENST00000520481.1:n.54+7G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.306+7G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.306+7G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.284+7G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.342+7G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.342+7G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.222+7G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.342+7G>A
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2796
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40947
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2241
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 5.25e1
  variant carriers: 0
hgvs: c.342+7G>A
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

8-28321123-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321123
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321123
    reference: chr 8
allele count: 1
allele frequency: 8.485218748939348e-6
allele num: 117852
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.222+6G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.306+6G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.306+6G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.342+6G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.284+6G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000520481
  gene symbol: FBXO16
  hgvsc: ENST00000520481.1:n.54+6G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.342+6G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.342+6G>A
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14089
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34045
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1245
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1966
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1558
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1181
  bin: 3.25e1
  variant carriers: 0
hgvs: c.342+6G>A
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD

8-28321131-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321131
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321131
    reference: chr 8
allele count: 1
allele frequency: 8.428434165500733e-6
allele num: 118646
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.304C>T
  hgvsp: ENSP00000429687.1:p.Gln102Ter
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.340C>T
  hgvsp: ENSP00000429390.1:p.Gln114Ter
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.282C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.340C>T
  hgvsp: ENSP00000369604.2:p.Gln114Ter
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.340C>T
  hgvsp: ENSP00000428902.1:p.Gln114Ter
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.220C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000520481
  gene symbol: FBXO16
  hgvsc: ENST00000520481.1:n.52C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.304C>T
  hgvsp: ENSP00000341416.2:p.Gln102Ter
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14665
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 573
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41983
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln114Ter
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

8-28321133-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321133
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321133
    reference: chr 8
allele count: 1
allele frequency: 8.423606314335294e-6
allele num: 118714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.302C>T
  hgvsp: ENSP00000341416.2:p.Ala101Val
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.302C>T
  hgvsp: ENSP00000429687.1:p.Ala101Val
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.218C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.338C>T
  hgvsp: ENSP00000429390.1:p.Ala113Val
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.338C>T
  hgvsp: ENSP00000428902.1:p.Ala113Val
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000520481
  gene symbol: FBXO16
  hgvsc: ENST00000520481.1:n.50C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.280C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.338C>T
  hgvsp: ENSP00000369604.2:p.Ala113Val
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34302
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4352
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1124
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1967
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 678
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 386
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1599
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 898
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala113Val
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum

8-28321134-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321134
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321134
    reference: chr 8
allele count: 2
allele frequency: 1.683785149014986e-5
allele num: 118780
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.279G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.337G>A
  hgvsp: ENSP00000369604.2:p.Ala113Thr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000520481
  gene symbol: FBXO16
  hgvsc: ENST00000520481.1:n.49G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.337G>A
  hgvsp: ENSP00000429390.1:p.Ala113Thr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.301G>A
  hgvsp: ENSP00000341416.2:p.Ala101Thr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.301G>A
  hgvsp: ENSP00000429687.1:p.Ala101Thr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.217G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.337G>A
  hgvsp: ENSP00000428902.1:p.Ala113Thr
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34199
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14994
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1632
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1788
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala113Thr
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-28321135-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321135
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321135
    reference: chr 8
allele count: 2
allele frequency: 1.682170673036486e-5
allele num: 118894
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.336T>G
  hgvsp: ENSP00000369604.2:p.Cys112Trp
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.300T>G
  hgvsp: ENSP00000341416.2:p.Cys100Trp
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.336T>G
  hgvsp: ENSP00000429390.1:p.Cys112Trp
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.300T>G
  hgvsp: ENSP00000429687.1:p.Cys100Trp
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000520481
  gene symbol: FBXO16
  hgvsc: ENST00000520481.1:n.48T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.216T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.336T>G
  hgvsp: ENSP00000428902.1:p.Cys112Trp
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.278T>G
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4309
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34234
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1139
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 259
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1630
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41811
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Cys112Trp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-28321137-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321137
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321137
    reference: chr 8
allele count: 1
allele frequency: 8.401949252226517e-6
allele num: 119020
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.298T>G
  hgvsp: ENSP00000341416.2:p.Cys100Gly
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.334T>G
  hgvsp: ENSP00000369604.2:p.Cys112Gly
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000520481
  gene symbol: FBXO16
  hgvsc: ENST00000520481.1:n.46T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.276T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.298T>G
  hgvsp: ENSP00000429687.1:p.Cys100Gly
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.334T>G
  hgvsp: ENSP00000428902.1:p.Cys112Gly
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.334T>G
  hgvsp: ENSP00000429390.1:p.Cys112Gly
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.214T>G
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34266
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1648
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15199
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42287
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1638
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1806
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Cys112Gly
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum

8-28321139-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321139
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321139
    reference: chr 8
allele count: 5
allele frequency: 4.199351620109855e-5
allele num: 119066
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.296G>A
  hgvsp: ENSP00000429687.1:p.Arg99His
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.332G>A
  hgvsp: ENSP00000428902.1:p.Arg111His
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.332G>A
  hgvsp: ENSP00000429390.1:p.Arg111His
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.274G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.212G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000520481
  gene symbol: FBXO16
  hgvsc: ENST00000520481.1:n.44G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.296G>A
  hgvsp: ENSP00000341416.2:p.Arg99His
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.332G>A
  hgvsp: ENSP00000369604.2:p.Arg111His
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15317
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4389
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1176
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34159
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5619
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 604
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1475
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42174
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1971
  bin: 9.75e1
  variant carriers: 5
hgvs: p.Arg111His
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

8-28321145-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321145
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321145
    reference: chr 8
allele count: 1
allele frequency: 8.368340892734607e-6
allele num: 119498
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.326T>C
  hgvsp: ENSP00000428902.1:p.Leu109Pro
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.268T>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.290T>C
  hgvsp: ENSP00000429687.1:p.Leu97Pro
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.326T>C
  hgvsp: ENSP00000429390.1:p.Leu109Pro
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.290T>C
  hgvsp: ENSP00000341416.2:p.Leu97Pro
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.206T>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.326T>C
  hgvsp: ENSP00000369604.2:p.Leu109Pro
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000520481
  gene symbol: FBXO16
  hgvsc: ENST00000520481.1:n.38T>C
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4457
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15893
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1275
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5714
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1793
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1970
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 711
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu109Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD

8-28321151-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321151
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321151
    reference: chr 8
allele count: 4
allele frequency: 3.341296757271497e-5
allele num: 119714
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.320G>A
  hgvsp: ENSP00000428902.1:p.Arg107Gln
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.262G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000520481
  gene symbol: FBXO16
  hgvsc: ENST00000520481.1:n.32G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.200G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.284G>A
  hgvsp: ENSP00000429687.1:p.Arg95Gln
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.320G>A
  hgvsp: ENSP00000429390.1:p.Arg107Gln
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.320G>A
  hgvsp: ENSP00000369604.2:p.Arg107Gln
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.284G>A
  hgvsp: ENSP00000341416.2:p.Arg95Gln
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4556
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33397
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 666
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1971
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1777
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1129
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg107Gln
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

8-28321152-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321152
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321152
    reference: chr 8
allele count: 3
allele frequency: 2.504884524823406e-5
allele num: 119766
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.283C>T
  hgvsp: ENSP00000341416.2:p.Arg95Trp
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000520481
  gene symbol: FBXO16
  hgvsc: ENST00000520481.1:n.31C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.319C>T
  hgvsp: ENSP00000369604.2:p.Arg107Trp
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.283C>T
  hgvsp: ENSP00000429687.1:p.Arg95Trp
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.319C>T
  hgvsp: ENSP00000429390.1:p.Arg107Trp
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.319C>T
  hgvsp: ENSP00000428902.1:p.Arg107Trp
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.199C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.261C>T
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16587
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1970
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5747
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg107Trp
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

8-28321153-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321153
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321153
    reference: chr 8
allele count: 2302
allele frequency: 1.918845025340091e-2
allele num: 119968
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.282T>C
  hgvsp: ENST00000518734.1:c.282T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.260T>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.318T>C
  hgvsp: ENST00000517673.1:c.318T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.198T>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000520481
  gene symbol: FBXO16
  hgvsc: ENST00000520481.1:n.30T>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.318T>C
  hgvsp: ENST00000521548.1:c.318T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.318T>C
  hgvsp: ENST00000380254.2:c.318T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.282T>C
  hgvsp: ENST00000346498.2:c.282T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 6.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 9.75e1
  variant carriers: 156
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 4.25e1
  variant carriers: 200
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 1.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 1.75e1
  variant carriers: 106
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 686
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 8.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 4639
  bin: 3.25e1
  variant carriers: 295
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 4.75e1
  variant carriers: 139
genotype depth: GenotypeDepth
  all individuals: 32578
  bin: 2.25e1
  variant carriers: 215
genotype depth: GenotypeDepth
  all individuals: 1431
  bin: 3.75e1
  variant carriers: 238
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 6.25e1
  variant carriers: 48
genotype depth: GenotypeDepth
  all individuals: 16533
  bin: 2.75e1
  variant carriers: 315
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 116
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1552
  bin: 7.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 4.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 8.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 503
  bin: 3.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 1
hgvs: p.Pro106Pro
num of homozygotes: 213
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum

8-28321156-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321156
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321156
    reference: chr 8
allele count: 9
allele frequency: 7.495877267502873e-5
allele num: 120066
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.257C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.315C>T
  hgvsp: ENST00000517673.1:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.279C>T
  hgvsp: ENST00000346498.2:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.279C>T
  hgvsp: ENST00000518734.1:c.279C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.315C>T
  hgvsp: ENST00000380254.2:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.315C>T
  hgvsp: ENST00000521548.1:c.315C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000520481
  gene symbol: FBXO16
  hgvsc: ENST00000520481.1:n.27C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.195C>T
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32521
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4648
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1393
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16858
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 549
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1812
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 492
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42062
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 339
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp105Asp
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP

8-28321157-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321157
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321157
    reference: chr 8
allele count: 2
allele frequency: 1.665528555487084e-5
allele num: 120082
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.278A>C
  hgvsp: ENSP00000429687.1:p.Asp93Ala
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.278A>C
  hgvsp: ENSP00000341416.2:p.Asp93Ala
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000520481
  gene symbol: FBXO16
  hgvsc: ENST00000520481.1:n.26A>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.314A>C
  hgvsp: ENSP00000428902.1:p.Asp105Ala
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.314A>C
  hgvsp: ENSP00000369604.2:p.Asp105Ala
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.314A>C
  hgvsp: ENSP00000429390.1:p.Asp105Ala
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.194A>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.256A>C
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1336
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4635
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32514
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1812
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 490
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1640
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 946
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp105Ala
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP

8-28321173-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321173
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321173
    reference: chr 8
allele count: 1
allele frequency: 8.300683976359652e-6
allele num: 120472
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.262A>G
  hgvsp: ENSP00000341416.2:p.Ile88Val
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.298A>G
  hgvsp: ENSP00000369604.2:p.Ile100Val
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.298A>G
  hgvsp: ENSP00000428902.1:p.Ile100Val
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000520481
  gene symbol: FBXO16
  hgvsc: ENST00000520481.1:n.10A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.240A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.262A>G
  hgvsp: ENSP00000429687.1:p.Ile88Val
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.178A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.298A>G
  hgvsp: ENSP00000429390.1:p.Ile100Val
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17791
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1641
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1132
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 637
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile100Val
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

8-28321174-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321174
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321174
    reference: chr 8
allele count: 2064
allele frequency: 1.71294836257407e-2
allele num: 120494
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.297C>T
  hgvsp: ENST00000380254.2:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.297C>T
  hgvsp: ENST00000521548.1:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.177C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.261C>T
  hgvsp: ENST00000518734.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000520481
  gene symbol: FBXO16
  hgvsc: ENST00000520481.1:n.9C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.297C>T
  hgvsp: ENST00000517673.1:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.261C>T
  hgvsp: ENST00000346498.2:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.239C>T
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.75e1
  variant carriers: 178
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 1.75e1
  variant carriers: 65
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.25e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 4787
  bin: 3.25e1
  variant carriers: 267
genotype depth: GenotypeDepth
  all individuals: 32153
  bin: 2.25e1
  variant carriers: 180
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.75e1
  variant carriers: 138
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.75e1
  variant carriers: 68
genotype depth: GenotypeDepth
  all individuals: 17712
  bin: 2.75e1
  variant carriers: 239
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 5.25e1
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 1430
  bin: 3.75e1
  variant carriers: 229
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 8.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 6.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 4.25e1
  variant carriers: 179
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 4.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 8.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1034
  bin: 8.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 4.25e1
  variant carriers: 3
hgvs: p.Tyr99Tyr
num of homozygotes: 163
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS

http://identifiers.org/exac.variant/8-28321188-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321188
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321188
    reference: chr 8
allele count: 1
allele frequency: 8.284180528862085e-6
allele num: 120712
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.247G>T
  hgvsp: ENSP00000341416.2:p.Val83Leu
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.283G>T
  hgvsp: ENSP00000428902.1:p.Val95Leu
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.247G>T
  hgvsp: ENSP00000429687.1:p.Val83Leu
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.225G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.283G>T
  hgvsp: ENSP00000369604.2:p.Val95Leu
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.163G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.283G>T
  hgvsp: ENSP00000429390.1:p.Val95Leu
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32265
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1641
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 222
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44284
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val95Leu
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-28321188-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321188
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321188
    reference: chr 8
allele count: 2
allele frequency: 1.656836105772417e-5
allele num: 120712
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.247G>A
  hgvsp: ENSP00000341416.2:p.Val83Met
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.163G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.225G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.283G>A
  hgvsp: ENSP00000369604.2:p.Val95Met
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.283G>A
  hgvsp: ENSP00000428902.1:p.Val95Met
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.283G>A
  hgvsp: ENSP00000429390.1:p.Val95Met
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.247G>A
  hgvsp: ENSP00000429687.1:p.Val83Met
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 560
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4902
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32265
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 532
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2001
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 371
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5903
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Val95Met
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD

8-28321197-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321197
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321197
    reference: chr 8
allele count: 1
allele frequency: 8.275131574592036e-6
allele num: 120844
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.154C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.238C>T
  hgvsp: ENSP00000341416.2:p.Leu80Phe
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.274C>T
  hgvsp: ENSP00000369604.2:p.Leu92Phe
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.274C>T
  hgvsp: ENSP00000429390.1:p.Leu92Phe
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.238C>T
  hgvsp: ENSP00000429687.1:p.Leu80Phe
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.274C>T
  hgvsp: ENSP00000428902.1:p.Leu92Phe
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.216C>T
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 18821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32251
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44976
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5976
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1105
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1637
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu92Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

8-28321197-G-GCGAAA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321197
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321202
    reference: chr 8
allele count: 1
allele frequency: 8.275131574592036e-6
allele num: 120844
alternate allele: GCGAAA
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.237_238insTTTCG
  hgvsp: ENSP00000429687.1:p.Leu80PhefsTer42
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.273_274insTTTCG
  hgvsp: ENSP00000428902.1:p.Leu92PhefsTer42
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.215_216insTTTCG
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.273_274insTTTCG
  hgvsp: ENSP00000429390.1:p.Leu92PhefsTer33
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.273_274insTTTCG
  hgvsp: ENSP00000369604.2:p.Leu92PhefsTer42
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.237_238insTTTCG
  hgvsp: ENSP00000341416.2:p.Leu80PhefsTer42
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.153_154insTTTCG
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32251
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5976
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 293
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1775
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Leu92PhefsTer42
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

8-28321228-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321228
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321228
    reference: chr 8
allele count: 3
allele frequency: 2.475860361475613e-5
allele num: 121170
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.243T>A
  hgvsp: ENST00000521548.1:c.243T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.243T>A
  hgvsp: ENST00000517673.1:c.243T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.185T>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.243T>A
  hgvsp: ENST00000380254.2:c.243T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.207T>A
  hgvsp: ENST00000346498.2:c.207T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.123T>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.207T>A
  hgvsp: ENST00000518734.1:c.207T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32285
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1112
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6084
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46305
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile81Ile
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum

8-28321229-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321229
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321228
    reference: chr 8
allele count: 1
allele frequency: 8.252050634582693e-6
allele num: 121182
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.241delA
  hgvsp: ENSP00000369604.2:p.Ile81PhefsTer51
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.205delA
  hgvsp: ENSP00000429687.1:p.Ile69PhefsTer51
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.205delA
  hgvsp: ENSP00000341416.2:p.Ile69PhefsTer51
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.241delA
  hgvsp: ENSP00000428902.1:p.Ile81PhefsTer51
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.241delA
  hgvsp: ENSP00000429390.1:p.Ile81PhefsTer42
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.183delA
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.121delA
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19647
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1641
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6084
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46297
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile81PhefsTer51
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: AT
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

8-28321238-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321238
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321238
    reference: chr 8
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.233A>G
  hgvsp: ENSP00000429390.1:p.Gln78Arg
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.197A>G
  hgvsp: ENSP00000429687.1:p.Gln66Arg
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.233A>G
  hgvsp: ENSP00000428902.1:p.Gln78Arg
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.197A>G
  hgvsp: ENSP00000341416.2:p.Gln66Arg
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.233A>G
  hgvsp: ENSP00000369604.2:p.Gln78Arg
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.175A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.113A>G
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32273
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1112
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6090
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 581
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1766
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gln78Arg
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

8-28321243-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321243
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321243
    reference: chr 8
allele count: 2
allele frequency: 1.650056101907465e-5
allele num: 121208
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.228G>A
  hgvsp: ENST00000517673.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.170G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.192G>A
  hgvsp: ENST00000518734.1:c.192G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.228G>A
  hgvsp: ENST00000521548.1:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.192G>A
  hgvsp: ENST00000346498.2:c.192G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.228G>A
  hgvsp: ENST00000380254.2:c.228G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.108G>A
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5122
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2001
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys76Lys
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum

8-28321247-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321247
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321247
    reference: chr 8
allele count: 639
allele frequency: 5.270885574765739e-3
allele num: 121232
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.224G>A
  hgvsp: ENSP00000369604.2:p.Arg75Gln
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.166G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.188G>A
  hgvsp: ENSP00000341416.2:p.Arg63Gln
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.104G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.188G>A
  hgvsp: ENSP00000429687.1:p.Arg63Gln
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.224G>A
  hgvsp: ENSP00000428902.1:p.Arg75Gln
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.224G>A
  hgvsp: ENSP00000429390.1:p.Arg75Gln
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 9.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31985
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 5.25e1
  variant carriers: 67
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 3.75e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 5051
  bin: 3.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 19665
  bin: 2.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 4.75e1
  variant carriers: 80
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 4.25e1
  variant carriers: 70
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5993
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1598
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg75Gln
num of homozygotes: 8
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS

8-28321248-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321248
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321248
    reference: chr 8
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.223C>T
  hgvsp: ENSP00000428902.1:p.Arg75Ter
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.223C>T
  hgvsp: ENSP00000429390.1:p.Arg75Ter
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.103C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.187C>T
  hgvsp: ENSP00000341416.2:p.Arg63Ter
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.165C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.223C>T
  hgvsp: ENSP00000369604.2:p.Arg75Ter
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.187C>T
  hgvsp: ENSP00000429687.1:p.Arg63Ter
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6106
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg75Ter
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum

8-28321248-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321248
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321248
    reference: chr 8
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.187C>A
  hgvsp: ENST00000346498.2:c.187C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.223C>A
  hgvsp: ENST00000521548.1:c.223C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.103C>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.223C>A
  hgvsp: ENST00000380254.2:c.223C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.223C>A
  hgvsp: ENST00000517673.1:c.223C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.187C>A
  hgvsp: ENST00000518734.1:c.187C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.165C>A
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1357
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1980
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1089
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6106
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1742
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg75Arg
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

8-28321249-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321249
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321249
    reference: chr 8
allele count: 9
allele frequency: 7.423782499670054e-5
allele num: 121232
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.222T>C
  hgvsp: ENST00000517673.1:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.222T>C
  hgvsp: ENST00000521548.1:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.102T>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.186T>C
  hgvsp: ENST00000346498.2:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.186T>C
  hgvsp: ENST00000518734.1:c.186T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.164T>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.222T>C
  hgvsp: ENST00000380254.2:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20010
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1986
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 46675
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6116
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1090
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Cys74Cys
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

8-28321252-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321252
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321252
    reference: chr 8
allele count: 1
allele frequency: 8.248375070111188e-6
allele num: 121236
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.183C>G
  hgvsp: ENSP00000341416.2:p.Cys61Trp
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.219C>G
  hgvsp: ENSP00000428902.1:p.Cys73Trp
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.161C>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.219C>G
  hgvsp: ENSP00000369604.2:p.Cys73Trp
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.183C>G
  hgvsp: ENSP00000429687.1:p.Cys61Trp
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.219C>G
  hgvsp: ENSP00000429390.1:p.Cys73Trp
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.99C>G
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20018
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46700
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6129
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Cys73Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS

8-28321253-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321253
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321253
    reference: chr 8
allele count: 14
allele frequency: 1.154810611059786e-4
allele num: 121232
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.218G>A
  hgvsp: ENSP00000369604.2:p.Cys73Tyr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.182G>A
  hgvsp: ENSP00000341416.2:p.Cys61Tyr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.218G>A
  hgvsp: ENSP00000428902.1:p.Cys73Tyr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.218G>A
  hgvsp: ENSP00000429390.1:p.Cys73Tyr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.182G>A
  hgvsp: ENSP00000429687.1:p.Cys61Tyr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.160G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.98G>A
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5148
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1351
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 32072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6137
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1085
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Cys73Tyr
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

http://identifiers.org/exac.variant/8-28321254-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321254
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321254
    reference: chr 8
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.97T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.217T>G
  hgvsp: ENSP00000429390.1:p.Cys73Gly
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.217T>G
  hgvsp: ENSP00000369604.2:p.Cys73Gly
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.159T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.181T>G
  hgvsp: ENSP00000429687.1:p.Cys61Gly
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.181T>G
  hgvsp: ENSP00000341416.2:p.Cys61Gly
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.217T>G
  hgvsp: ENSP00000428902.1:p.Cys73Gly
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20042
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1975
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46706
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Cys73Gly
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS

8-28321259-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321259
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321259
    reference: chr 8
allele count: 3
allele frequency: 2.47520667975776e-5
allele num: 121202
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.154A>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.212A>C
  hgvsp: ENSP00000429390.1:p.Lys71Thr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.212A>C
  hgvsp: ENSP00000428902.1:p.Lys71Thr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.212A>C
  hgvsp: ENSP00000369604.2:p.Lys71Thr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.176A>C
  hgvsp: ENSP00000429687.1:p.Lys59Thr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.92A>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.176A>C
  hgvsp: ENSP00000341416.2:p.Lys59Thr
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32048
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6140
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1738
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46708
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Lys71Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

8-28321265-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321265
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321265
    reference: chr 8
allele count: 2
allele frequency: 1.650873311982039e-5
allele num: 121148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.206A>T
  hgvsp: ENSP00000428902.1:p.Gln69Leu
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.206A>T
  hgvsp: ENSP00000429390.1:p.Gln69Leu
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.206A>T
  hgvsp: ENSP00000369604.2:p.Gln69Leu
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.170A>T
  hgvsp: ENSP00000429687.1:p.Gln57Leu
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.148A>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.86A>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.170A>T
  hgvsp: ENSP00000341416.2:p.Gln57Leu
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32001
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5143
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 604
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1974
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6110
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1086
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln69Leu
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD

8-28321268-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321268
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321268
    reference: chr 8
allele count: 1
allele frequency: 8.25695648583932e-6
allele num: 121110
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.203C>G
  hgvsp: ENSP00000428902.1:p.Ser68Cys
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.83C>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.167C>G
  hgvsp: ENSP00000429687.1:p.Ser56Cys
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.145C>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.203C>G
  hgvsp: ENSP00000369604.2:p.Ser68Cys
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.167C>G
  hgvsp: ENSP00000341416.2:p.Ser56Cys
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.203C>G
  hgvsp: ENSP00000429390.1:p.Ser68Cys
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31966
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5132
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1729
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ser68Cys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff

8-28321271-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321271
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321271
    reference: chr 8
allele count: 3
allele frequency: 2.477905344015859e-5
allele num: 121070
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.200T>C
  hgvsp: ENSP00000428902.1:p.Leu67Pro
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.164T>C
  hgvsp: ENSP00000429687.1:p.Leu55Pro
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.80T>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.164T>C
  hgvsp: ENSP00000341416.2:p.Leu55Pro
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.200T>C
  hgvsp: ENSP00000369604.2:p.Leu67Pro
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.200T>C
  hgvsp: ENSP00000429390.1:p.Leu67Pro
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.142T>C
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6085
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1606
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 320
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu67Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

8-28321273-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321273
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321273
    reference: chr 8
allele count: 5
allele frequency: 4.130251614928381e-5
allele num: 121058
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.198G>A
  hgvsp: ENST00000521548.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.78G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.162G>A
  hgvsp: ENST00000518734.1:c.162G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.162G>A
  hgvsp: ENST00000346498.2:c.162G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.198G>A
  hgvsp: ENST00000517673.1:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.198G>A
  hgvsp: ENST00000380254.2:c.198G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.140G>A
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5136
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1601
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser66Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

8-28321274-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321274
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321274
    reference: chr 8
allele count: 2
allele frequency: 1.652455548945733e-5
allele num: 121032
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.161C>T
  hgvsp: ENSP00000429687.1:p.Ser54Leu
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.197C>T
  hgvsp: ENSP00000369604.2:p.Ser66Leu
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.77C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.139C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.197C>T
  hgvsp: ENSP00000428902.1:p.Ser66Leu
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.161C>T
  hgvsp: ENSP00000341416.2:p.Ser54Leu
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.197C>T
  hgvsp: ENSP00000429390.1:p.Ser66Leu
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20033
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1600
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser66Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

8-28321275-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321275
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321275
    reference: chr 8
allele count: 1
allele frequency: 8.26255081468751e-6
allele num: 121028
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.160T>A
  hgvsp: ENSP00000341416.2:p.Ser54Thr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.196T>A
  hgvsp: ENSP00000369604.2:p.Ser66Thr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.160T>A
  hgvsp: ENSP00000429687.1:p.Ser54Thr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.196T>A
  hgvsp: ENSP00000428902.1:p.Ser66Thr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.76T>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.196T>A
  hgvsp: ENSP00000429390.1:p.Ser66Thr
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.138T>A
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1338
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1604
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1966
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 345
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 564
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ser66Thr
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum

8-28321280-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321280
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321280
    reference: chr 8
allele count: 122
allele frequency: 1.008814725387401e-3
allele num: 120934
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.191G>A
  hgvsp: ENSP00000369604.2:p.Arg64His
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.155G>A
  hgvsp: ENSP00000429687.1:p.Arg52His
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.133G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.191G>A
  hgvsp: ENSP00000428902.1:p.Arg64His
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.155G>A
  hgvsp: ENSP00000341416.2:p.Arg52His
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.191G>A
  hgvsp: ENSP00000429390.1:p.Arg64His
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.71G>A
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 5.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19975
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 3.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1701
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 420
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46498
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg64His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

8-28321281-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321281
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321281
    reference: chr 8
allele count: 1
allele frequency: 8.271845945141119e-6
allele num: 120892
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.190C>T
  hgvsp: ENSP00000428902.1:p.Arg64Cys
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.190C>T
  hgvsp: ENSP00000429390.1:p.Arg64Cys
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.154C>T
  hgvsp: ENSP00000341416.2:p.Arg52Cys
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.190C>T
  hgvsp: ENSP00000369604.2:p.Arg64Cys
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.132C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.154C>T
  hgvsp: ENSP00000429687.1:p.Arg52Cys
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.70C>T
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1593
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg64Cys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

8-28321284-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321284
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321284
    reference: chr 8
allele count: 2
allele frequency: 1.654889370645572e-5
allele num: 120854
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.187G>A
  hgvsp: ENSP00000369604.2:p.Glu63Lys
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.129G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.187G>A
  hgvsp: ENSP00000429390.1:p.Glu63Lys
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.187G>A
  hgvsp: ENSP00000428902.1:p.Glu63Lys
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.67G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.151G>A
  hgvsp: ENSP00000341416.2:p.Glu51Lys
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.151G>A
  hgvsp: ENSP00000429687.1:p.Glu51Lys
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20014
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1335
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 463
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1703
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Glu63Lys
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: MQ

8-28321301-ATTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321301
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321298
    reference: chr 8
allele count: 9
allele frequency: 7.476449185067039e-5
allele num: 120378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.131_133delGAA
  hgvsp: ENSP00000341416.2:p.Arg44del
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.167_169delGAA
  hgvsp: ENSP00000428902.1:p.Arg56del
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.47_49delGAA
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.167_169delGAA
  hgvsp: ENSP00000369604.2:p.Arg56del
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.167_169delGAA
  hgvsp: ENSP00000429390.1:p.Arg56del
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.109_111delGAA
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.131_133delGAA
  hgvsp: ENSP00000429687.1:p.Arg44del
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5025
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31635
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1965
  bin: 9.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 776
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5994
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg56del
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: Other
reference allele: ATTC
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

8-28321314-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321314
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321314
    reference: chr 8
allele count: 13
allele frequency: 1.084417751084418e-4
allele num: 119880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.99C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.157C>T
  hgvsp: ENSP00000369604.2:p.Gln53Ter
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.37C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.157C>T
  hgvsp: ENSP00000429390.1:p.Gln53Ter
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.121C>T
  hgvsp: ENSP00000429687.1:p.Gln41Ter
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.121C>T
  hgvsp: ENSP00000341416.2:p.Gln41Ter
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.157C>T
  hgvsp: ENSP00000428902.1:p.Gln53Ter
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31271
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19653
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5002
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1324
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45707
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5900
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 458
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1968
  bin: 9.75e1
  variant carriers: 13
hgvs: p.Gln53Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

8-28321320-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321320
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321320
    reference: chr 8
allele count: 1
allele frequency: 8.365120792344242e-6
allele num: 119544
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.31G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.151G>A
  hgvsp: ENSP00000369604.2:p.Asp51Asn
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.115G>A
  hgvsp: ENSP00000341416.2:p.Asp39Asn
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.115G>A
  hgvsp: ENSP00000429687.1:p.Asp39Asn
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.93G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.151G>A
  hgvsp: ENSP00000428902.1:p.Asp51Asn
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.151G>A
  hgvsp: ENSP00000429390.1:p.Asp51Asn
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19517
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1646
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45282
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1529
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp51Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum

8-28321335-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321335
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321335
    reference: chr 8
allele count: 1
allele frequency: 8.452942469273554e-6
allele num: 118302
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136T>A
  hgvsp: ENSP00000369604.2:p.Phe46Ile
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100T>A
  hgvsp: ENSP00000429687.1:p.Phe34Ile
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136T>A
  hgvsp: ENSP00000428902.1:p.Phe46Ile
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78T>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100T>A
  hgvsp: ENSP00000341416.2:p.Phe34Ile
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16T>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136T>A
  hgvsp: ENSP00000429390.1:p.Phe46Ile
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4878
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1305
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29489
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 579
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 334
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Phe46Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

8-28321338-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321338
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321338
    reference: chr 8
allele count: 1
allele frequency: 8.477737461426295e-6
allele num: 117956
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-3C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-3C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-3C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-3C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-3C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-3C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-3C>T
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1314
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18695
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 451
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1581
  bin: 7.75e1
  variant carriers: 0
hgvs: c.136-3C>T
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

http://identifiers.org/exac.variant/8-28321343-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321343
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321343
    reference: chr 8
allele count: 1171
allele frequency: 9.995902618909414e-3
allele num: 117148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-8G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-8G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-8G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-8G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-8G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-8G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-8G>T
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 7.5e0
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 3785
  bin: 1.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 1326
  bin: 3.75e1
  variant carriers: 152
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 1.75e1
  variant carriers: 86
genotype depth: GenotypeDepth
  all individuals: 4756
  bin: 3.25e1
  variant carriers: 173
genotype depth: GenotypeDepth
  all individuals: 27600
  bin: 2.25e1
  variant carriers: 146
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.25e1
  variant carriers: 93
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 2.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 4.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 18012
  bin: 2.75e1
  variant carriers: 194
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 9.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 5.25e1
  variant carriers: 36
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 8.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1491
  bin: 7.75e1
  variant carriers: 16
genotype quality: GenotypeQuality
  all individuals: 2803
  bin: 9.75e1
  variant carriers: 1070
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5270
  bin: 6.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 9.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 1390
  bin: 7.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
hgvs: c.136-8G>T
num of homozygotes: 54
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

http://identifiers.org/exac.variant/8-28321345-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321345
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321345
    reference: chr 8
allele count: 1
allele frequency: 8.638861052558831e-6
allele num: 115756
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-10G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-10G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-10G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-10G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-10G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-10G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-10G>T
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1292
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25000
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6032
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4836
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1665
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1539
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2005
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 512
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1270
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 528
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 959
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

8-28321348-A-ACACACACATATACACACATATACACAAACACAAATATACACACAAACACACAT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321348
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321401
    reference: chr 8
allele count: 1
allele frequency: 8.635578583765113e-6
allele num: 115800
alternate allele: ACACACACATATACACACATATACACAAACACAAATATACACACAAACACACAT
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17201
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6024
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 958
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 409
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1787
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1399
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4507
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1021
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1217
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36945
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

8-28321351-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321351
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321351
    reference: chr 8
allele count: 1
allele frequency: 8.651716500553709e-6
allele num: 115584
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-16T>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-16T>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-16T>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-16T>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-16T>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-16T>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-16T>C
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2292
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16876
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 548
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 955
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37073
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
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  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1391
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5452
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

8-28321353-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321353
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321352
    reference: chr 8
allele count: 2
allele frequency: 1.737830839546079e-5
allele num: 115086
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-19delC
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-19delC
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-19delC
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-19delC
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-19delC
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-19delC
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-19delC
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15875
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7857
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
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  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23961
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34211
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1783
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 6077
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 557
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 588
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1891
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1251
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: AG
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

8-28321355-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321355
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321355
    reference: chr 8
allele count: 1
allele frequency: 8.71368571478364e-6
allele num: 114762
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-20G>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-20G>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-20G>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-20G>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-20G>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-20G>C
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-20G>C
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6325
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1807
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4233
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2027
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum

8-28321355-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321355
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321355
    reference: chr 8
allele count: 22
allele frequency: 1.917010857252401e-4
allele num: 114762
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-20G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-20G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-20G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-20G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-20G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-20G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-20G>A
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3440
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15506
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 614
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23334
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6325
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1968
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 370
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3079
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 948
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2027
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33603
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD

8-28321372-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321372
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321372
    reference: chr 8
allele count: 1
allele frequency: 8.937988237607479e-6
allele num: 111882
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-37G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-37G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-37G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-37G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-37G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-37G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-37G>A
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14780
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 919
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13041
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1004
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3623
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 460
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2919
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6524
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3093
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16541
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

8-28321374-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321374
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321374
    reference: chr 8
allele count: 1
allele frequency: 8.971828458639871e-6
allele num: 111460
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-39C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-39C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-39C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-39C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-39C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-39C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-39C>T
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12965
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3628
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16066
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13429
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14675
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 911
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6857
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1027
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3241
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7344
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1289
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3951
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD

8-28321377-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28321377
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28321377
    reference: chr 8
allele count: 1
allele frequency: 8.992805755395683e-6
allele num: 111200
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-42A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-42A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-42A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-42A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-42A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-42A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-42A>G
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12897
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2647
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16592
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7651
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1785
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1065
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6996
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3728
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7079
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3418
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

8-28322842-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28322842
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28322842
    reference: chr 8
allele count: 1
allele frequency: 1.240079365079365e-4
allele num: 8064
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-1507C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-1507C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-1507C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-1507C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428683
  ensembl transcript: ENST00000519471
  gene symbol: FBXO16
  hgvsc: ENST00000519471.2:c.*46C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-1507C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-1507C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-1507C>T
  variant of: http://identifiers.org/hgnc/13618
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 3.25e1
  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: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1110
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1706
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

8-28322842-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28322842
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28322842
    reference: chr 8
allele count: 2
allele frequency: 2.48015873015873e-4
allele num: 8064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-1507C>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-1507C>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-1507C>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428683
  ensembl transcript: ENST00000519471
  gene symbol: FBXO16
  hgvsc: ENST00000519471.2:c.*46C>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-1507C>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-1507C>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-1507C>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-1507C>A
  variant of: http://identifiers.org/hgnc/13618
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2286
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1989
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 477
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

8-28322856-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28322856
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28322856
    reference: chr 8
allele count: 5
allele frequency: 5.949547834364588e-4
allele num: 8404
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-1521A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428683
  ensembl transcript: ENST00000519471
  gene symbol: FBXO16
  hgvsc: ENST00000519471.2:c.*32A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-1521A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-1521A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-1521A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-1521A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-1521A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-1521A>G
  variant of: http://identifiers.org/hgnc/13618
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  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: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1690
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1062
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 6.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

8-28322864-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28322864
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28322864
    reference: chr 8
allele count: 403
allele frequency: 4.4947579745706e-2
allele num: 8966
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-1529C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-1529C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428683
  ensembl transcript: ENST00000519471
  gene symbol: FBXO16
  hgvsc: ENST00000519471.2:c.*24C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-1529C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-1529C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-1529C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-1529C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-1529C>T
  variant of: http://identifiers.org/hgnc/13618
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 7.5e0
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 2.5e0
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1481
  bin: 1.25e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 1.75e1
  variant carriers: 154
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1533
  bin: 2.25e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 2.75e1
  variant carriers: 35
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 9.75e1
  variant carriers: 357
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 7.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 1557
  bin: 7.5e0
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1049
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 571
  bin: 3.25e1
  variant carriers: 2
num of homozygotes: 12
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ

8-28322882-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28322882
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28322882
    reference: chr 8
allele count: 7
allele frequency: 7.421543681085666e-4
allele num: 9432
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-1547C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-1547C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-1547C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-1547C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428683
  ensembl transcript: ENST00000519471
  gene symbol: FBXO16
  hgvsc: ENST00000519471.2:c.*6C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-1547C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-1547C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-1547C>T
  variant of: http://identifiers.org/hgnc/13618
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1873
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2264
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 1.25e1
  variant carriers: 2
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: 8
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 419
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2514
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 336
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

8-28322918-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28322918
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28322918
    reference: chr 8
allele count: 1
allele frequency: 9.66183574879227e-5
allele num: 10350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-1583A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-1583A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-1583A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428683
  ensembl transcript: ENST00000519471
  gene symbol: FBXO16
  hgvsc: ENST00000519471.2:c.180A>G
  hgvsp: ENST00000519471.2:c.180A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-1583A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-1583A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-1583A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-1583A>G
  variant of: http://identifiers.org/hgnc/13618
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4477
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg60Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

8-28322922-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28322922
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28322922
    reference: chr 8
allele count: 4
allele frequency: 3.856536829926726e-4
allele num: 10372
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428683
  ensembl transcript: ENST00000519471
  gene symbol: FBXO16
  hgvsc: ENST00000519471.2:c.176A>G
  hgvsp: ENSP00000428683.2:p.Lys59Arg
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-1587A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-1587A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-1587A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-1587A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-1587A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-1587A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-1587A>G
  variant of: http://identifiers.org/hgnc/13618
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1511
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1488
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4503
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 382
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys59Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP

8-28322949-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28322949
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28322949
    reference: chr 8
allele count: 6
allele frequency: 5.778120184899846e-4
allele num: 10384
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-1614C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-1614C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428683
  ensembl transcript: ENST00000519471
  gene symbol: FBXO16
  hgvsc: ENST00000519471.2:c.149C>T
  hgvsp: ENSP00000428683.2:p.Ser50Leu
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-1614C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-1614C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-1614C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-1614C>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-1614C>T
  variant of: http://identifiers.org/hgnc/13618
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2939
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 185
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1403
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser50Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD

8-28322957-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28322957
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28322957
    reference: chr 8
allele count: 2
allele frequency: 1.948937828883259e-4
allele num: 10262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-1622G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-1622G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-1622G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-1622G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-1622G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-1622G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-1622G>A
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428683
  ensembl transcript: ENST00000519471
  gene symbol: FBXO16
  hgvsc: ENST00000519471.2:c.141G>A
  hgvsp: ENST00000519471.2:c.141G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13618
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2673
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1626
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1368
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4213
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly47Gly
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
reference allele: C
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/8-28322960-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28322960
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28322960
    reference: chr 8
allele count: 4
allele frequency: 3.939334252511325e-4
allele num: 10154
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428683
  ensembl transcript: ENST00000519471
  gene symbol: FBXO16
  hgvsc: ENST00000519471.2:c.138G>T
  hgvsp: ENSP00000428683.2:p.Met46Ile
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-1625G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-1625G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-1625G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-1625G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-1625G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-1625G>T
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-1625G>T
  variant of: http://identifiers.org/hgnc/13618
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2505
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Met46Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP

8-28322965-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28322965
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28322965
    reference: chr 8
allele count: 0
allele frequency: 0.0e0
allele num: 9944
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-1630C>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428683
  ensembl transcript: ENST00000519471
  gene symbol: FBXO16
  hgvsc: ENST00000519471.2:c.136-3C>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-1630C>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-1630C>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-1630C>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-1630C>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-1630C>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-1630C>G
  variant of: http://identifiers.org/hgnc/13618
canonical: false
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 937
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1360
  bin: 7.5e0
  variant carriers: 0
hgvs: c.136-3C>G
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-28322978-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28322978
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28322978
    reference: chr 8
allele count: 1
allele frequency: 1.110864252388358e-4
allele num: 9002
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-1643T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-1643T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-1643T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-1643T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-1643T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428683
  ensembl transcript: ENST00000519471
  gene symbol: FBXO16
  hgvsc: ENST00000519471.2:c.136-16T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-1643T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-1643T>G
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 397
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2093
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

8-28323008-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28323008
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28323008
    reference: chr 8
allele count: 1
allele frequency: 1.667778519012675e-4
allele num: 5996
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.100-1673A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.136-1673A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428683
  ensembl transcript: ENST00000519471
  gene symbol: FBXO16
  hgvsc: ENST00000519471.2:c.136-46A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.16-1673A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.78-1673A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.100-1673A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.136-1673A>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.136-1673A>G
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1941
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2252
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 623
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 379
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 587
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/8-28331241-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 28331241
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 28331241
    reference: chr 8
allele count: 1
allele frequency: 8.29228651508367e-6
allele num: 120594
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428683
  ensembl transcript: ENST00000519471
  gene symbol: FBXO16
  hgvsc: ENST00000519471.2:c.135+48T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429687
  ensembl transcript: ENST00000518734
  gene symbol: FBXO16
  hgvsc: ENST00000518734.1:c.99+9624T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000518016
  gene symbol: FBXO16
  hgvsc: ENST00000518016.1:n.15+48T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000428902
  ensembl transcript: ENST00000521548
  gene symbol: FBXO16
  hgvsc: ENST00000521548.1:c.135+48T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000429390
  ensembl transcript: ENST00000517673
  gene symbol: FBXO16
  hgvsc: ENST00000517673.1:c.135+48T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000369604
  ensembl transcript: ENST00000380254
  gene symbol: FBXO16
  hgvsc: ENST00000380254.2:c.135+48T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl transcript: ENST00000517436
  gene symbol: FBXO16
  hgvsc: ENST00000517436.1:n.77+48T>G
  variant of: http://identifiers.org/hgnc/13618
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000214050
  ensembl protein: ENSP00000341416
  ensembl transcript: ENST00000346498
  gene symbol: FBXO16
  hgvsc: ENST00000346498.2:c.99+9624T>G
  variant of: http://identifiers.org/hgnc/13618
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10625
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7868
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6978
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4090
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12673
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2666
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1277
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3216
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum

GenotypeQuality
all individuals: 574
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

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

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

GenotypeQuality
all individuals: 462
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1016
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1548
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1110
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 354
bin: 4.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64774
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10006
num of homozygotes: 0

East Asian
type: Population
allele count: 9
allele frequency: 1.072961373390558e-3
allele num: 8388
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15918
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11032
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6510
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

MQ
type: SiteQuality
SIO_000300: 5.931e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.75e-1

FS
type: SiteQuality
SIO_000300: 5.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e-1

DP
type: SiteQuality
SIO_000300: 1.441228e6

MQRankSum
type: SiteQuality
SIO_000300: 1.2e-1

QD
type: SiteQuality
SIO_000300: 9.970000000000001e0

VQSLOD
type: SiteQuality
SIO_000300: 1.03e0

GenotypeQuality
all individuals: 1546
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1242
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1755
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1109
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 934
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5370
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.189060642092747e-4
allele num: 8410
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15926
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10018
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11056
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64906
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.904e1

VQSLOD
type: SiteQuality
SIO_000300: -3.555e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.544e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.425e0

MQRankSum
type: SiteQuality
SIO_000300: -7.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.124e0

QD
type: SiteQuality
SIO_000300: 1.175e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

DP
type: SiteQuality
SIO_000300: 1.44906e6

GenotypeQuality
all individuals: 1763
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 884
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5388
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1121
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 531
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 811
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41195
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8420
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10032
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64980
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.271951831409934e-5
allele num: 15944
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11078
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.16e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.406e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.15e0

MQ
type: SiteQuality
SIO_000300: 5.861e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.357e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.456e0

DP
type: SiteQuality
SIO_000300: 1.452696e6

QD
type: SiteQuality
SIO_000300: 1.302e1

GenotypeQuality
all individuals: 5516
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1783
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 925
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1128
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1719
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1593
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 4.75e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65388
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11198
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8450
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.228977201943441e-5
allele num: 16054
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.827e0

DP
type: SiteQuality
SIO_000300: 1.470429e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.4e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 2.27e0

QD
type: SiteQuality
SIO_000300: 1.252e1

GenotypeQuality
all individuals: 23
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 41938
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5535
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1664
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1789
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 648
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65430
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11224
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16056
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.526717557251908e-4
allele num: 6550
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.81e-1

DP
type: SiteQuality
SIO_000300: 1.473686e6

QD
type: SiteQuality
SIO_000300: 1.051e1

MQ
type: SiteQuality
SIO_000300: 5.925e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.566e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.7e-2

FS
type: SiteQuality
SIO_000300: 1.101e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

GenotypeQuality
all individuals: 41925
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 610
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5574
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 658
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1134
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 869
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1607
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10128
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8450
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16066
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.054927598215922e-5
allele num: 65468
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11226
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 9.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.590000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.474907e6

MQ
type: SiteQuality
SIO_000300: 5.861e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.434e0

MQRankSum
type: SiteQuality
SIO_000300: -7.3e-2

FS
type: SiteQuality
SIO_000300: 3.963e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.068e0

GenotypeQuality
all individuals: 1606
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5607
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1968
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 450
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1800
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.051571559353067e-4
allele num: 6554
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8460
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10146
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16080
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11232
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65536
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.04e-1

FS
type: SiteQuality
SIO_000300: 7.81e-1

QD
type: SiteQuality
SIO_000300: 1.264e1

DP
type: SiteQuality
SIO_000300: 1.475689e6

MQ
type: SiteQuality
SIO_000300: 5.958e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

GenotypeQuality
all individuals: 805
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5624
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1533
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1132
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 488
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 4.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65610
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.211951795254069e-5
allele num: 16098
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11250
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

QD
type: SiteQuality
SIO_000300: 1.236e1

DP
type: SiteQuality
SIO_000300: 1.478955e6

FS
type: SiteQuality
SIO_000300: 6.558e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.81e-1

GenotypeQuality
all individuals: 584
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 576
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 643
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 409
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1129
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1790
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1637
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16100
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.970831690973591e-4
allele num: 10148
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8472
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.047015448368323e-5
allele num: 65638
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.884150675195451e-5
allele num: 11256
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.43e0

DP
type: SiteQuality
SIO_000300: 1.482461e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.25e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.817e0

FS
type: SiteQuality
SIO_000300: 1.8161e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.147e0

GenotypeQuality
all individuals: 376
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1135
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 803
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42240
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 3.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65838
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.123595505617978e-3
allele num: 890
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.726e0

FS
type: SiteQuality
SIO_000300: 4.859e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: 3.75e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.929999999999999e-1

DP
type: SiteQuality
SIO_000300: 1.491196e6

QD
type: SiteQuality
SIO_000300: 1.581e1

GenotypeQuality
all individuals: 29
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 510
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1124
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 483
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1641
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5721
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42487
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.233197681588359e-4
allele num: 16218
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.123595505617978e-3
allele num: 890
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.177301624676242e-4
allele num: 8494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65980
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 4.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

MQRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

DP
type: SiteQuality
SIO_000300: 1.499445e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.195e0

QD
type: SiteQuality
SIO_000300: 1.33e1

GenotypeQuality
all individuals: 655
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1116
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1784
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1121
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42143
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 801
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16220
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11356
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.782821365681862e-5
allele num: 10222
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.030578537442798e-5
allele num: 65994
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.500636e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.47e0

MQRankSum
type: SiteQuality
SIO_000300: 2.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.62e-1

FS
type: SiteQuality
SIO_000300: 4.671e0

VQSLOD
type: SiteQuality
SIO_000300: 7.38e-1

QD
type: SiteQuality
SIO_000300: 1.007e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeQuality
all individuals: 550
bin: 9.25e1
variant carriers: 16

GenotypeQuality
all individuals: 3670
bin: 9.75e1
variant carriers: 1944

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 2.75e1
variant carriers: 5

GenotypeQuality
all individuals: 589
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 630
bin: 5.25e1
variant carriers: 12

GenotypeQuality
all individuals: 1685
bin: 7.75e1
variant carriers: 15

GenotypeQuality
all individuals: 550
bin: 4.75e1
variant carriers: 10

GenotypeQuality
all individuals: 1052
bin: 8.25e1
variant carriers: 15

GenotypeQuality
all individuals: 1009
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 41802
bin: 6.25e1
variant carriers: 13

GenotypeQuality
all individuals: 5562
bin: 6.75e1
variant carriers: 15

GenotypeQuality
all individuals: 285
bin: 5.75e1
variant carriers: 10

Latino
type: Population
allele count: 87
allele frequency: 7.653061224489796e-3
allele num: 11368
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 51
allele frequency: 7.720020586721565e-4
allele num: 66062
num of homozygotes: 0

African
type: Population
allele count: 2109
allele frequency: 2.044000775344059e-1
allele num: 10318
num of homozygotes: 212

East Asian
type: Population
allele count: 41
allele frequency: 4.822394730651611e-3
allele num: 8502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

Other
type: Population
allele count: 10
allele frequency: 1.118568232662192e-2
allele num: 894
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.463357556349304e-4
allele num: 16238
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.962e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.541e-1

FS
type: SiteQuality
SIO_000300: 5.53e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.52e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.14e0

VQSLOD
type: SiteQuality
SIO_000300: 5.92e0

MQRankSum
type: SiteQuality
SIO_000300: 6.8e-2

DP
type: SiteQuality
SIO_000300: 1.54013e6

QD
type: SiteQuality
SIO_000300: 1.305e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.999999999999999e-3

GenotypeQuality
all individuals: 971
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 693
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 439
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1650
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2510
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 1142
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5730
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66100
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16262
num of homozygotes: 0

African
type: Population
allele count: 8
allele frequency: 7.738440704198104e-4
allele num: 10338
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.793527963418924e-5
allele num: 11372
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.381e1

MQRankSum
type: SiteQuality
SIO_000300: -7.6e-2

FS
type: SiteQuality
SIO_000300: 1.154e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.54e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.452e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

DP
type: SiteQuality
SIO_000300: 1.534503e6

GenotypeQuality
all individuals: 5743
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 588
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1138
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2505
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 633
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42337
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.025535519787002e-5
allele num: 66104
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10344
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.078e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

MQRankSum
type: SiteQuality
SIO_000300: 5.97e-1

FS
type: SiteQuality
SIO_000300: 8.420999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.312e1

DP
type: SiteQuality
SIO_000300: 1.535294e6

GenotypeQuality
all individuals: 425
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43650
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5725
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 696
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2502
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1798
bin: 7.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11430
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16356
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508159140952553e-5
allele num: 66306
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.185e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.83e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.87e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.99e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.71e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.548446e6

GenotypeQuality
all individuals: 314
bin: 5.25e1
variant carriers: 8

GenotypeQuality
all individuals: 406
bin: 3.25e1
variant carriers: 2

GenotypeQuality
all individuals: 305
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 43458
bin: 6.25e1
variant carriers: 8

GenotypeQuality
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 550
bin: 9.25e1
variant carriers: 11

GenotypeQuality
all individuals: 5
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5576
bin: 6.75e1
variant carriers: 14

GenotypeQuality
all individuals: 3541
bin: 9.75e1
variant carriers: 1810

GenotypeQuality
all individuals: 403
bin: 3.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1546
bin: 7.25e1
variant carriers: 3

GenotypeQuality
all individuals: 1654
bin: 7.75e1
variant carriers: 11

Latino
type: Population
allele count: 72
allele frequency: 6.298110566829951e-3
allele num: 11432
num of homozygotes: 0

East Asian
type: Population
allele count: 40
allele frequency: 4.681647940074907e-3
allele num: 8544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 47
allele frequency: 7.087279088002895e-4
allele num: 66316
num of homozygotes: 0

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

African
type: Population
allele count: 1891
allele frequency: 1.825994592506759e-1
allele num: 10356
num of homozygotes: 163

South Asian
type: Population
allele count: 4
allele frequency: 2.445884798825975e-4
allele num: 16354
num of homozygotes: 0

Other
type: Population
allele count: 10
allele frequency: 1.116071428571429e-2
allele num: 896
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.96e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.677e0

DP
type: SiteQuality
SIO_000300: 1.563939e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.337e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

QD
type: SiteQuality
SIO_000300: 1.189e1

VQSLOD
type: SiteQuality
SIO_000300: 3.79e0

FS
type: SiteQuality
SIO_000300: 2.553e0

GenotypeQuality
all individuals: 267
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2001
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1769
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1109
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 582
bin: 9.25e1
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GenotypeQuality
all individuals: 250
bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16408
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505479947007106e-5
allele num: 66424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

FS
type: SiteQuality
SIO_000300: 2.639e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

QD
type: SiteQuality
SIO_000300: 1.001e1

DP
type: SiteQuality
SIO_000300: 1.533876e6

VQSLOD
type: SiteQuality
SIO_000300: -5.49e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.512e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.27e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.010959894014212e-5
allele num: 66424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -5.49e-2

MQRankSum
type: SiteQuality
SIO_000300: -9.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e0

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.639e0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.512e0

QD
type: SiteQuality
SIO_000300: 1.001e1

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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bin: 2.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.169043722235212e-4
allele num: 8554
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.656e0

DP
type: SiteQuality
SIO_000300: 1.538908e6

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.362e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8554
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504121292341014e-5
allele num: 66484
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16440
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.362e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -5.0e-2

QD
type: SiteQuality
SIO_000300: 9.539999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.29e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.656e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

DP
type: SiteQuality
SIO_000300: 1.538908e6

GenotypeQuality
all individuals: 1
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
all individuals: 90
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.819725827975252e-4
allele num: 16486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.05e1

VQSLOD
type: SiteQuality
SIO_000300: -1.855e-1

MQ
type: SiteQuality
SIO_000300: 5.961e1

DP
type: SiteQuality
SIO_000300: 1.552236e6

FS
type: SiteQuality
SIO_000300: 6.24e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.919e0

GenotypeQuality
all individuals: 2002
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variant carriers: 1

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-1

MQ
type: SiteQuality
SIO_000300: 6.008e1

FS
type: SiteQuality
SIO_000300: 2.078e0

MQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.311e1

DP
type: SiteQuality
SIO_000300: 1.552522e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.51e0

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499835018148004e-5
allele num: 66674
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele num: 904
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South Asian
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QD
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SIO_000300: 1.401e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.838e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

DP
type: SiteQuality
SIO_000300: 1.55408e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1108
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.212856276531231e-4
allele num: 16490
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.118e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.898e0

DP
type: SiteQuality
SIO_000300: 1.554772e6

ClippingRankSum
type: SiteQuality
SIO_000300: 4.37e-1

FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 4.1e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 42
allele frequency: 3.638253638253638e-3
allele num: 11544
num of homozygotes: 0

Other
type: Population
allele count: 5
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allele num: 908
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African
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allele count: 7
allele frequency: 6.75414897722887e-4
allele num: 10364
num of homozygotes: 0

South Asian
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allele count: 92
allele frequency: 5.578462284744118e-3
allele num: 16492
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European (Finnish)
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allele count: 7
allele frequency: 1.059963658388855e-3
allele num: 6604
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East Asian
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allele count: 252
allele frequency: 2.920046349942063e-2
allele num: 8630
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European (Non-Finnish)
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allele count: 234
allele frequency: 3.508771929824561e-3
allele num: 66690
num of homozygotes: 2

QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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MQ
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InbreedingCoeff
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1980
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GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 908
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East Asian
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allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQ
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QD
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DP
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.06e-1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -5.21e-1

MQRankSum
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SIO_000300: 2.39e-1

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

African
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allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

South Asian
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allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

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

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

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

Latino
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allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.04972707096155e-4
allele num: 66684
num of homozygotes: 0

European (Finnish)
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allele count: 2
allele frequency: 3.027550711474417e-4
allele num: 6606
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

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

MQ
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SIO_000300: 6.0e1

MQRankSum
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InbreedingCoeff
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SIO_000300: -3.0e-4

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66684
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 6.06060606060606e-5
allele num: 16500
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African
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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MQRankSum
type: SiteQuality
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InbreedingCoeff
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QD
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ClippingRankSum
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SIO_000300: -1.15e-1

DP
type: SiteQuality
SIO_000300: 1.557189e6

FS
type: SiteQuality
SIO_000300: 2.209e0

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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bin: 4.75e1
variant carriers: 0

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

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

South Asian
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allele frequency: 0.0e0
allele num: 16500
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East Asian
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allele count: 14
allele frequency: 1.621872103799815e-3
allele num: 8632
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66686
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

QD
type: SiteQuality
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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DP
type: SiteQuality
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FS
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.277e0

MQRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.499610101373643e-5
allele num: 66684
num of homozygotes: 0

East Asian
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num of homozygotes: 0

InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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MQ
type: SiteQuality
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DP
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MQRankSum
type: SiteQuality
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QD
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ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

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

South Asian
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allele frequency: 1.818402230573403e-4
allele num: 16498
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66672
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Latino
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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VQSLOD
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FS
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BaseQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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QD
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MQRankSum
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DP
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ClippingRankSum
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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

South Asian
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 3.000300030003e-5
allele num: 66660
num of homozygotes: 0

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

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

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

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.502476361999099e-5
allele num: 66630
num of homozygotes: 0

African
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Other
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East Asian
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allele frequency: 0.0e0
allele num: 8622
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Latino
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allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

South Asian
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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FS
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VQSLOD
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QD
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DP
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MQ
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ReadPosRankSum
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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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bin: 1.75e1
variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 10274
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 908
num of homozygotes: 0

East Asian
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allele count: 3
allele frequency: 3.479471120389701e-4
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.001921229586936e-5
allele num: 66624
num of homozygotes: 0

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

QD
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FS
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ClippingRankSum
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SIO_000300: -4.04e-1

ReadPosRankSum
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MQ
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SIO_000300: 6.0e1

MQRankSum
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BaseQRankSum
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SIO_000300: -4.06e-1

VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.554324e6

GenotypeQuality
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variant carriers: 2

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

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66620
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 2.321262766945218e-4
allele num: 8616
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.938e1

QD
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MQRankSum
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DP
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FS
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10260
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.955e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.654e0

VQSLOD
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DP
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FS
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SIO_000300: 6.65e-1

QD
type: SiteQuality
SIO_000300: 1.151e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e-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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variant carriers: 122

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

European (Non-Finnish)
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allele count: 104
allele frequency: 1.561936801634026e-3
allele num: 66584
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

European (Finnish)
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allele count: 1
allele frequency: 1.516530178950561e-4
allele num: 6594
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

Latino
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allele count: 15
allele frequency: 1.300954032957502e-3
allele num: 11530
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.93e-1

FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.198e1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.0e-1

MQ
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SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 4.24e0

MQRankSum
type: SiteQuality
SIO_000300: 2.46e-1

DP
type: SiteQuality
SIO_000300: 1.55599e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-2

GenotypeQuality
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variant carriers: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66564
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.162250116225012e-4
allele num: 8604
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African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.319e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.07e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.97e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.18e0

DP
type: SiteQuality
SIO_000300: 1.551652e6

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 (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

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

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

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

East Asian
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allele count: 2
allele frequency: 2.325040688212044e-4
allele num: 8602
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66558
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66378
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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African
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East Asian
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allele count: 9
allele frequency: 1.052877866167525e-3
allele num: 8548
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South Asian
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Other
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InbreedingCoeff
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FS
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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MQ
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MQRankSum
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DP
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 11
allele frequency: 1.663490911290567e-4
allele num: 66126
num of homozygotes: 0

Other
type: Population
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Latino
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allele frequency: 8.736676568233443e-5
allele num: 11446
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East Asian
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European (Finnish)
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African
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allele num: 9868
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South Asian
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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DP
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FS
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
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MQ
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 65986
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Other
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East Asian
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South Asian
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European (Finnish)
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African
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Latino
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FS
type: SiteQuality
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QD
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BaseQRankSum
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DP
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ClippingRankSum
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MQ
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65332
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African
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16354
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.846426043878273e-5
allele num: 11304
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8368
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.890000000000001e0

FS
type: SiteQuality
SIO_000300: 3.038e0

MQRankSum
type: SiteQuality
SIO_000300: -1.141e0

VQSLOD
type: SiteQuality
SIO_000300: -2.193e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.409999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.18e0

MQ
type: SiteQuality
SIO_000300: 5.94e1

DP
type: SiteQuality
SIO_000300: 1.500829e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 151
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6538
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.124448799608035e-5
allele num: 16328
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8330
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65130
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11278
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.181e0

MQRankSum
type: SiteQuality
SIO_000300: -1.465e0

DP
type: SiteQuality
SIO_000300: 1.492475e6

MQ
type: SiteQuality
SIO_000300: 5.956e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.343e1

VQSLOD
type: SiteQuality
SIO_000300: -3.945e-1

GenotypeQuality
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bin: 5.25e1
variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8242
num of homozygotes: 0

Latino
type: Population
allele count: 37
allele frequency: 3.297682709447415e-3
allele num: 11220
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.146281499692685e-5
allele num: 16270
num of homozygotes: 0

Other
type: Population
allele count: 6
allele frequency: 6.787330316742082e-3
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 1111
allele frequency: 1.185699039487727e-1
allele num: 9370
num of homozygotes: 54

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.475477302967479e-4
allele num: 64634
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.468916e6

FS
type: SiteQuality
SIO_000300: 1.878e0

VQSLOD
type: SiteQuality
SIO_000300: 3.77e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.65e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.39e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.69e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.418e0

GenotypeQuality
all individuals: 413
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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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variant carriers: 0

GenotypeQuality
all individuals: 1400
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63876
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9048
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11128
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.171315724512466e-5
allele num: 16204
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 4.789e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.71e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.734e0

DP
type: SiteQuality
SIO_000300: 1.418712e6

VQSLOD
type: SiteQuality
SIO_000300: -9.563e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.39e-1

QD
type: SiteQuality
SIO_000300: 3.063e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 527
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16210
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8124
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11126
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.564945226917058e-5
allele num: 63900
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 5.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.41e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.377e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQ
type: SiteQuality
SIO_000300: 5.408e1

FS
type: SiteQuality
SIO_000300: 2.131e1

MQRankSum
type: SiteQuality
SIO_000300: -4.899e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.529e0

QD
type: SiteQuality
SIO_000300: 7.7e-1

DP
type: SiteQuality
SIO_000300: 1.41267e6

GenotypeQuality
all individuals: 1782
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 526
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1258
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2142
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8106
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16202
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9026
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.000900090009001e-5
allele num: 11110
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63768
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.401698e6

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.73e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.61e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 4.576e0

QD
type: SiteQuality
SIO_000300: 1.638e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.88e-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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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8052
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.236399604352127e-4
allele num: 16176
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8958
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11050
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

DP
type: SiteQuality
SIO_000300: 1.373728e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.76e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.107e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.3e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.807e1

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8924
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 63302
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11026
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8024
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.194251734390486e-5
allele num: 16144
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e-1

DP
type: SiteQuality
SIO_000300: 1.363532e6

FS
type: SiteQuality
SIO_000300: 3.611e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11026
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.120573733751681e-4
allele num: 8924
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.545595054095827e-4
allele num: 6470
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16144
num of homozygotes: 0

European (Non-Finnish)
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allele count: 20
allele frequency: 3.159457837035165e-4
allele num: 63302
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8024
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Other
type: Population
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.61e-1

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

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.363532e6

QD
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 758
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61584
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 1
allele frequency: 6.261740763932373e-5
allele num: 15970
num of homozygotes: 0

Other
type: Population
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allele num: 854
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10702
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.630151278038602e-5
allele num: 61344
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7676
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15966
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

DP
type: SiteQuality
SIO_000300: 1.183209e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.91e-1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -1.191e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.6e-2

QD
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SIO_000300: 6.04e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.906e1

VQSLOD
type: SiteQuality
SIO_000300: -1.824e0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 10672
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.634574520252378e-5
allele num: 61178
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15940
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.173889e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

QD
type: SiteQuality
SIO_000300: 1.757e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: -2.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.1e-2

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 5590
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2014
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

African
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allele count: 1
allele frequency: 5.681818181818182e-3
allele num: 176
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 82
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.868e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.03e-2

MQRankSum
type: SiteQuality
SIO_000300: -2.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
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SIO_000300: -1.306e0

FS
type: SiteQuality
SIO_000300: 4.833e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

QD
type: SiteQuality
SIO_000300: 8.039999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

DP
type: SiteQuality
SIO_000300: 8.1251e4

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 126
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.136363636363636e-2
allele num: 176
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 82
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5590
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2014
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.306e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.89e-1

QD
type: SiteQuality
SIO_000300: 8.039999999999999e0

FS
type: SiteQuality
SIO_000300: 4.833e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.868e0

DP
type: SiteQuality
SIO_000300: 8.1251e4

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.03e-2

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 5
allele frequency: 2.808988764044944e-2
allele num: 178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5822
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 80
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 130
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 76
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2118
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

MQRankSum
type: SiteQuality
SIO_000300: -1.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.64e-2

QD
type: SiteQuality
SIO_000300: 1.333e1

FS
type: SiteQuality
SIO_000300: 3.297e0

DP
type: SiteQuality
SIO_000300: 8.6781e4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 4

Latino
type: Population
allele count: 4
allele frequency: 5.0e-2
allele num: 80
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 32
allele frequency: 1.441441441441441e-2
allele num: 2220
num of homozygotes: 0

African
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allele count: 27
allele frequency: 1.51685393258427e-1
allele num: 178
num of homozygotes: 2

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 11
allele frequency: 8.333333333333333e-2
allele num: 132
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.333333333333333e-2
allele num: 90
num of homozygotes: 0

South Asian
type: Population
allele count: 326
allele frequency: 5.202681136291095e-2
allele num: 6266
num of homozygotes: 10

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

QD
type: SiteQuality
SIO_000300: 1.398e1

DP
type: SiteQuality
SIO_000300: 9.425e4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

VQSLOD
type: SiteQuality
SIO_000300: 6.5e0

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 6
allele frequency: 2.551020408163265e-3
allele num: 2352
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African
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South Asian
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allele frequency: 1.519756838905775e-4
allele num: 6580
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 84
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FS
type: SiteQuality
SIO_000300: 1.975e0

MQRankSum
type: SiteQuality
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ReadPosRankSum
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QD
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VQSLOD
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: -3.14e-2

MQ
type: SiteQuality
SIO_000300: 5.953e1

DP
type: SiteQuality
SIO_000300: 1.06187e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7230
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 132
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African
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allele count: 1
allele frequency: 5.319148936170213e-3
allele num: 188
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 92
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

ReadPosRankSum
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SIO_000300: 2.84e-1

FS
type: SiteQuality
SIO_000300: 3.315e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-2

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.938e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

DP
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SIO_000300: 1.2911e5

BaseQRankSum
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SIO_000300: 2.77e0

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

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

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 2598
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South Asian
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allele frequency: 5.518763796909492e-4
allele num: 7248
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Latino
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allele frequency: 0.0e0
allele num: 92
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
type: SiteQuality
SIO_000300: -7.45e-1

BaseQRankSum
type: SiteQuality
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VQSLOD
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FS
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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ClippingRankSum
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InbreedingCoeff
type: SiteQuality
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QD
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DP
type: SiteQuality
SIO_000300: 1.29557e5

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 116
num of homozygotes: 0

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